[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"enhanced-recovery-after-surgery\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:enhanced-recovery-after-surgery":35},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,14,0,[8,53,88,117,144,172,198,225,251,284,306,338,363,386],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":39,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":49,"locationsCount":52},"100642312","risk-factors-of-atrial-fibrillation-after-cardiac-surgery-100642312",false,"NCT07625033","Risk Factors of Atrial Fibrillation After Cardiac Surgery","PFAS","Inclusion Criteria:\n\n* age \\>18\n* having undergone a scheduled cardiac surgery in the study center\n* having agreed to the reuse of their hospital care data\n\nExclusion Criteria:\n\n* Atrial fibrillation at the admission in hospital.","ALL","18 Years",{"count":19,"type":20},918,"ESTIMATED","OBSERVATIONAL","Supraventricular arrhythmias complicate more than 40% of cardiac surgeries and are associated with an increased risk of bleeding, stroke, heart failure, and death. Preventing the occurrence of these arrhythmias is a major challenge. This study aims to investigate risk factors and protective factors regarding atrial fibrillation and other iatrogenic cardiac arrhythmias after cardiac surgery, particularly innovative anesthetic strategies such as stellar ganglion blockade which have been recently implemented in our center.",[24,25,26,27,28,29,30,31,32,33,34,35,36,37,38],"Cardiac Surgery","Peri Operative Medicine","Thoracic Surgery","Cardiopulmonary Bypass","Coronary Artery Bypass","Heart Valve Prosthesis Implantation","Aortic Valve Replacement","Perioperative Medicine","Preoperative Care","Intraoperative Care","Postoperative Care","Enhanced Recovery After Surgery","Anesthesia","Cardiac Anesthesia","Intensive Care Unit",[40],"Stellar Ganglion Blockade, SGB, cardiac surgery","NOT_YET_RECRUITING","2026-06-23",{"date":44,"type":45},"2026-06-25","ACTUAL",{"date":47,"type":20},"2026-07-01",{"date":47,"type":20},{"name":50,"class":51},"Centre Hospitalier Régional Metz-Thionville","OTHER",1,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":16,"minAge":60,"maxAge":61,"enrollmentInfo":62,"targetDuration":4,"studyType":64,"phases":65,"briefSummary":67,"conditions":68,"keywords":73,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":52},"100637651","phase-4-transversus-abdominis-plane-and-rectus-sheath-block-for-robotic-colectomy-100637651","NCT07624916","Transversus Abdominis Plane and Rectus Sheath Block for Robotic Colectomy","Impact of Transversus Abdominis Plane Block Combined With Rectus Sheath Block on Postoperative Pain Management in Patients Undergoing Elective Robotic Colectomy","Inclusion Criteria:\n\n* Patients scheduled for elective robotic colorectal cancer surgery for the first time\n\nExclusion Criteria:\n\n* Age \\\u003C 18 years or age \\> 80 years\n* Allergic to any medication in the protocol\n* Infection over the injection site\n* Chronic pain history\n* Severe hepatic or renal insufficiency\n* Pregnancy\n* Emergency surgery\n* Refusal to join the study","20 Years","80 Years",{"count":63,"type":20},90,"INTERVENTIONAL",[66],"PHASE4","This study aimed to evaluate the impact of ultrasound-guided bilateral transversus abdominis plane block combined with rectus sheath block on postoperative pain and recovery after robotic colectomy under an enhanced recovery after surgery (ERAS) protocol.",[69,70,35,71,72],"Rectus Sheath Block","Transversus Abdominis Plane Block","Robotic Surgery","Colorectal Cancer",[74,75,76,77,78],"colorectal cancer","robotic colectomy","enhanced recovery after surgery","transversus abdominis plane block","rectus sheath block","2026-05-30",{"date":81,"type":45},"2026-06-03",{"date":83,"type":20},"2026-06-01",{"date":85,"type":20},"2028-03-31",{"name":87,"class":51},"Tri-Service General Hospital",{"id":89,"slug":90,"hasResults":11,"nctId":91,"briefTitle":92,"officialTitle":93,"acronym":4,"eligibilityCriteria":94,"healthyVolunteers":11,"sex":95,"minAge":17,"maxAge":4,"enrollmentInfo":96,"targetDuration":4,"studyType":64,"phases":98,"briefSummary":100,"conditions":101,"keywords":4,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":52},"100467293","prehabilitation-for-ovarian-cancer-patients-100467293","NCT05364879","Prehabilitation for Ovarian Cancer Patients","The Impact of Prehabilitation Exercise on Frailty and Treatment Outcomes in Ovarian Cancer Patients","Inclusion Criteria:\n\n* 18 years or older\n* Have a confirmed diagnosis of stage III or IV ovarian cancer\n* Scheduled to receive cytoreductive surgery as part of their treatment plan\n* Must have a minimum of 4-weeks between the time of study enrollment and scheduled surgery\n* Be able to attend in-person and\u002For virtual exercise sessions\n* Be fluent in English\n* Have oncologist approval\n\nExclusion Criteria:\n\n* Have already completed surgery\n* Unstable cardiac or respiratory disease, injury or any other co-morbid disease that may make it unsafe for participants to exercise\n* Significant cognitive impairment (e.g., do not have the capacity to consent, unable to follow exercise instructions)","FEMALE",{"count":97,"type":20},108,[99],"NA","Individuals with ovarian cancer have very poor survival rates. This is because the cancer is not usually detected until it has reached advanced stages. How long an individual survives also is determined by the cancer treatment they receive. Although there are best treatment practices to improve survival, some women have other conditions that limit treatment options. One such condition seen in as many as 50% of women with advanced ovarian cancer is frailty (an age-related decline in function and health). This is a major concern as doctors will often have to change how the cancer is treated based on the patient being frail. For example, patients living with frailty are less likely to have their full tumor removed during surgery. They are also more likely to have complications with surgery, stay in the hospital longer, and recover less well from surgery overall. Patients living with frailty also are more likely to experience delays in their chemotherapy starting, receive lower doses of chemotherapy and\u002For receive fewer cycles of chemotherapy. These changes in treatment may decrease how long a patient survives after diagnosis. Thus, research is needed to explore strategies to decrease frailty in patients who require treatment for advanced ovarian cancer. An option gaining more attention is physical exercise (e.g. walking, repeatedly rising from a chair). Exercise performed before surgery, which is called prehabilitation, can improve how well a patient recovers after surgery and increase how long they survive. Research has shown that prehabilitation is very beneficial for patients undergoing surgery for heart disease. However, it is not clear whether prehabilitation works for those with advanced ovarian cancer that are going to have surgery. Therefore, the investigators want to explore how a 4+ week exercise program performed while waiting for surgery for advanced ovarian cancer changes frailty and how a patient recovers after surgery. The investigators will specifically look whether the exercise program: 1) reduces how frail a patient is before surgery; 2) improves how well the patient recovers after surgery; and 3) affects the patient's chemotherapy treatment plan. This study will provide important information about the ability of prehabilitation exercise to improve surgical and treatment outcomes in women with advanced ovarian cancer. Overall, it is believed that exercise has the potential to improve the survival of advanced ovarian cancer patients.",[102,103,104,105,106,107,35],"Prehabilitation","Exercise","Frailty","Ovarian Cancer","Surgical Complication","Treatment Outcomes","RECRUITING","2026-05-28",{"date":83,"type":45},{"date":112,"type":45},"2023-01-03",{"date":114,"type":20},"2027-08-31",{"name":116,"class":51},"Nova Scotia Health Authority",{"id":118,"slug":119,"hasResults":11,"nctId":120,"briefTitle":121,"officialTitle":122,"acronym":123,"eligibilityCriteria":124,"healthyVolunteers":125,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":126,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":128,"conditions":129,"keywords":132,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":136,"lastUpdatePostDateStruct":137,"startDateStruct":139,"completionDateStruct":140,"leadSponsor":142,"locationsCount":52},"100639259","rideclas-delphi-classification-of-rica-pathway-recommendations-100639259","NCT07615855","RIDECLAS: Delphi Classification of RICA Pathway Recommendations","Delphi Study for the Classification of Recommendations for the RICA Pathway (Enhanced Recovery in Adult Surgery)","RIDECLAS","Inclusion Criteria:\n\n* Healthcare professional or researcher with relevant clinical or scientific experience in enhanced recovery pathways, perioperative medicine, surgery, anesthesiology, nursing, rehabilitation, or related disciplines.\n\nAt least 5 years of professional experience. Membership in GERM or participation in professional networks related to enhanced recovery in adult surgery.\n\nWillingness to participate in the planned Delphi rounds. Provision of electronic informed consent.\n\nExclusion Criteria:\n\n* Failure to meet the predefined professional experience criteria. Failure to provide informed consent. Failure to complete the first Delphi round. Duplicate or incomplete responses that cannot be validated for analysis.",true,{"count":127,"type":20},384,"RIDECLAS is an observational, prospective, non-interventional consensus study using a modified Delphi methodology. The study aims to obtain expert consensus on the classification and final formulation of recommendations for the RICA Pathway, an enhanced recovery pathway for adult surgery. Participants will be healthcare professionals with experience in enhanced recovery, perioperative medicine, surgery, anesthesiology, nursing, rehabilitation, or related disciplines. Experts will complete sequential online questionnaires. Individual responses will remain confidential, and aggregated anonymized feedback will be provided between Delphi rounds. The study does not involve patients, clinical interventions, biological samples, drugs, or medical devices.",[35,130,131],"Perioperative Care","Surgical Care",[133,134,135,31],"ERAS","Delphi Technique","RICA Pathway","2026-05-22",{"date":138,"type":45},"2026-05-29",{"date":83,"type":20},{"date":141,"type":20},"2026-12-31",{"name":143,"class":51},"Universidad de Zaragoza",{"id":145,"slug":146,"hasResults":11,"nctId":147,"briefTitle":148,"officialTitle":149,"acronym":4,"eligibilityCriteria":150,"healthyVolunteers":11,"sex":16,"minAge":151,"maxAge":4,"enrollmentInfo":152,"targetDuration":4,"studyType":64,"phases":154,"briefSummary":155,"conditions":156,"keywords":158,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":162,"lastUpdatePostDateStruct":163,"startDateStruct":165,"completionDateStruct":167,"leadSponsor":169,"locationsCount":171},"100591786","effectiveness-of-eras-on-postoperative-recovery-after-minimally-invasive-gastrectomy-100591786","NCT06984952","Effectiveness of ERAS on Postoperative Recovery After Minimally Invasive Gastrectomy","Effectiveness of Enhanced Recovery After Surgery (ERAS) on Postoperative Recovery After Minimally Invasive Gastrectomy: A Multi-center Open-labeled Randomized Controlled Study","Inclusion Criteria:\n\n* Adults aged ≥19 years scheduled to undergo elective laparoscopic or robotic gastrectomy for gastric cancer\n* American Society of Anesthesiologists physical status classification I to III\n* Ability to provide written informed consent, demonstrate understanding of the study protocol, and complete patient-reported outcome measures appropriately\n\nExclusion Criteria:\n\n* Requirement for resection of organs other than the stomach during surgery (except for cholecystectomy)\n* History of upper abdominal surgery (except for cholecystectomy)\n* Known hypersensitivity to fentanyl, ropivacaine, acetaminophen, or non-steroidal anti-inflammatory drugs\n* Determined by the investigator or study personnel to be otherwise unsuitable for participation in the study","19 Years",{"count":153,"type":20},308,[99],"This prospective, randomized, open-label, multicenter study is designed to evaluate the impact of an enhanced recovery after surgery (ERAS) protocol on the rate of meeting discharge criteria in patients undergoing minimally-invasive gastrectomy for gastric cancer. We hypothesize that implementation of our ERAS protocol will significantly increase the proportion of patients who meet standardized discharge criteria following minimally-invasive gastrectomy.",[35,157],"Gastrectomy for Gastric Cancer",[76,159,160,161],"stomach neoplasms","gastrectomy for gastric cancer","pain, postoperative","2025-09-04",{"date":164,"type":45},"2025-09-05",{"date":166,"type":45},"2025-06-13",{"date":168,"type":20},"2029-03-31",{"name":170,"class":51},"Seoul National University Hospital",10,{"id":173,"slug":174,"hasResults":11,"nctId":175,"briefTitle":176,"officialTitle":177,"acronym":178,"eligibilityCriteria":179,"healthyVolunteers":11,"sex":16,"minAge":180,"maxAge":4,"enrollmentInfo":181,"targetDuration":4,"studyType":64,"phases":183,"briefSummary":184,"conditions":185,"keywords":4,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":189,"lastUpdatePostDateStruct":190,"startDateStruct":192,"completionDateStruct":194,"leadSponsor":196,"locationsCount":4},"100597296","staircase-nutritional-intervention-for-elderly-patients-undergoing-spinal-fusion-surgery-100597296","NCT07056647","Staircase Nutritional Intervention for Elderly Patients Undergoing Spinal Fusion Surgery","A Prospective Multicenter Randomized Controlled Trial of a Staircase Nutritional Intervention Strategy Versus Conventional ERAS Diet Management for Elderly Patients Undergoing Spinal Fusion Surgery","SNIEPUSFS","Inclusion Criteria:\n\n* Age and Gender: Aged ≥ 75 years, regardless of gender. Surgery Type: Scheduled for elective spinal fusion surgery, including but not limited to lumbar, thoracic, and cervical spinal fusion surgeries. The surgeries are aimed at treating spinal degenerative diseases (such as lumbar disc herniation, lumbar spinal stenosis, etc.), spinal trauma, spinal deformities, etc.\n\nNutritional Status: Willing and able to cooperate with nutritional assessments (such as Mini - Nutritional Assessment, MNA), and patients with any level of nutritional risk are included.\n\nPhysical Condition: American Society of Anesthesiologists (ASA) physical status classification Ⅰ - Ⅲ, meaning the physical condition is relatively tolerable for surgery, without severe failure of important organs such as the heart, lungs, liver, and kidneys, and without uncontrolled severe hypertension, diabetic ketoacidosis, and other acute complications.\n\nCognitive and Communication Ability: Possessing basic cognitive and communication abilities, being able to understand the purpose, process, and relevant requirements of the study, and signing a written informed consent form.\n\nLife Expectancy: With a life expectancy of more than 1 year to facilitate long - term postoperative follow - up and assessment.\n\nExclusion Criteria:\n\n* Severe Underlying Diseases: Presence of severe heart failure (New York Heart Association functional class Ⅳ), end - stage liver disease (such as decompensated liver cirrhosis with severe ascites, hepatic encephalopathy, etc.), end - stage renal disease (requiring maintenance dialysis treatment), end - stage malignant tumors, and other serious underlying diseases that severely affect life and health and recovery.\n\nPsychiatric and Neurological Diseases: Suffering from severe mental illnesses (such as schizophrenia, major depressive disorder in the acute phase and unable to cooperate with the study), Alzheimer's disease and unable to understand the content of the study, and serious neurological diseases (such as long - term bedridden patients with severe stroke and impaired consciousness).\n\nContraindications to Nutritional Supplements: Allergic to the components of the nutritional supplements involved in the study (such as enteral nutrition powder mixture, low - sugar whole - protein enteral nutrition powder, etc.) or having severe intolerance.\n\nRecent Special Situations: Having a history of severe trauma or major surgery (other than the planned spinal fusion surgery) in the past 3 months; having a history of severe gastrointestinal diseases such as gastrointestinal bleeding and intestinal obstruction in the past 1 month.\n\nOthers: Currently participating in other clinical trials that may affect the results of this study; having insurmountable compliance problems (such as failure to take nutritional supplements on time, refusal of follow - up, etc.).","75 Years",{"count":182,"type":20},88,[99],"The goal of this prospective multicenter randomized controlled clinical trial is to evaluate the efficacy of a staircase nutritional intervention in reducing postoperative complications and improving long-term functional recovery in elderly patients aged ≥75 years scheduled for spinal fusion surgery. The main questions it aims to answer are:\n\n1. Does the staircase nutritional intervention reduce the 30-day postoperative complication rate, as measured by the Comprehensive Complication Index (CCI), compared to conventional ERAS diet management?\n2. Does the staircase nutritional intervention improve 1-year functional recovery, as assessed by Oswestry\u002FNeck Disability Index (ODI\u002FNDI) and health-related quality of life (EQ-5D), compared to conventional ERAS diet management?\n\nResearchers will compare the intervention group receiving MNA - based staircase nutritional intervention (including 14-day preadmission oral nutritional supplementation, perioperative personalized nutritional support, and postdischarge continuous management) combined with surgery-specific prehabilitation training to the control group receiving conventional ERAS diet management to see if the former leads to better clinical outcomes and long-term functional recovery.\n\nParticipants will\n\nUndergo randomization: Be randomly assigned to either the intervention group or the control group.\n\nReceive assigned interventions:\n\nControl group: Receive conventional ERAS diet management, including preadmission nutritional education and early postoperative oral intake.\n\nIntervention group: Undergo MNA - based staircase nutritional intervention and surgery-specific prehabilitation training.\n\nParticipate in follow-up: Complete short-term (within 90 days postoperatively) and long-term (6 and 12 months postoperatively) follow-up assessments, including laboratory tests, functional evaluations, and satisfaction surveys.",[186,187,188,35],"Nutritional Intervention","Spinal Surgery","Elderly","2025-06-29",{"date":191,"type":45},"2025-07-09",{"date":193,"type":20},"2025-07-01",{"date":195,"type":20},"2028-01-31",{"name":197,"class":51},"Xuanwu Hospital, Beijing",{"id":199,"slug":200,"hasResults":11,"nctId":201,"briefTitle":202,"officialTitle":203,"acronym":4,"eligibilityCriteria":204,"healthyVolunteers":11,"sex":95,"minAge":205,"maxAge":206,"enrollmentInfo":207,"targetDuration":4,"studyType":64,"phases":209,"briefSummary":210,"conditions":211,"keywords":213,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":216,"lastUpdatePostDateStruct":217,"startDateStruct":219,"completionDateStruct":221,"leadSponsor":223,"locationsCount":52},"100436477","eras-in-pediatric--adolescent-gynecology-preoperative-counseling-100436477","NCT04963751","ERAS in Pediatric & Adolescent Gynecology Preoperative Counseling","ERAS in Pediatric and Adolescent Gynecology: How Important is Preoperative Counseling in Patient Outcomes and Does Parent Versus Patient Counseling Impact Success?","Inclusion Criteria:\n\n* 9- 17 years of age\n* Patient is undergoing abdominal surgery and being managed under the ERAS protocol\n\nExclusion Criteria:\n\n* Developmental delay (IQ \\\u003C 70) determined by documentation in medical record\n* Emergency or non-elective surgical cases\n* Patients who attend clinic appointments independently from their caregiver","9 Years","17 Years",{"count":208,"type":20},60,[99],"The Investigator propose a randomized trial that will assess whether participant involvement in pre-operative counseling for ERAS improves post-surgical pain scores. The Investigator will also assess participant compliance to ERAS-prescribed medications, and functionality (return to school). Each participant who is enrolled in the study will be assigned to 1) pre-operative counseling with participant's caregiver or 2) caregiver-only counseling.",[35,212],"Gynecologic Disease",[214,133,215],"Gynecology","Pediatrics","2025-05-05",{"date":218,"type":45},"2025-05-06",{"date":220,"type":45},"2022-09-08",{"date":222,"type":20},"2027-06-30",{"name":224,"class":51},"University of Colorado, Denver",{"id":226,"slug":227,"hasResults":11,"nctId":228,"briefTitle":229,"officialTitle":230,"acronym":4,"eligibilityCriteria":231,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":232,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":234,"conditions":235,"keywords":238,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":242,"lastUpdatePostDateStruct":243,"startDateStruct":245,"completionDateStruct":247,"leadSponsor":249,"locationsCount":52},"100587981","effect-of-an-enhanced-recovery-after-surgery-program-on-outcomes-after-pancreatoduodenectomy-100587981","NCT06935448","Effect of an Enhanced Recovery After Surgery Program on Outcomes After Pancreatoduodenectomy","Effect of an Enhanced Recovery After Surgery Program on Outcomes After Pancreatoduodenectomy; Experience From Two Referral Centers in Central Greece.","Inclusion Criteria:\n\n* adult patients\n* diagnosis of pancreatic cancer\n* elective open pancreatic surgery\n\nExclusion Criteria:\n\n* age \\\u003C18 years\n* emergency pancreatic surgery\n* other surgical procedures\n* missing data\n* lost to follow-up",{"count":233,"type":20},170,"This study assesses whether patients with pancreatic cancer who undergo surgery experience improved outcomes following the implementation of a multidisciplinary care pathway, specifically an enhanced recovery after surgery (ERAS) program.\n\nThis pathway includes various interventions in the preoperative, intraoperative, and postoperative care of these patients, all aimed at enhancing their health status and postoperative results.",[236,35,237],"Pancreatectomy","Pancreatic Cancer Resectable",[239,76,240,241],"pancreatectomy","pancreatic cancer resectable","outcomes research","2025-04-16",{"date":244,"type":45},"2025-04-20",{"date":246,"type":45},"2019-07-01",{"date":248,"type":20},"2025-05-30",{"name":250,"class":51},"University of Thessaly",{"id":252,"slug":253,"hasResults":11,"nctId":254,"briefTitle":255,"officialTitle":256,"acronym":4,"eligibilityCriteria":257,"healthyVolunteers":11,"sex":16,"minAge":258,"maxAge":259,"enrollmentInfo":260,"targetDuration":4,"studyType":64,"phases":262,"briefSummary":263,"conditions":264,"keywords":270,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":275,"lastUpdatePostDateStruct":276,"startDateStruct":278,"completionDateStruct":280,"leadSponsor":282,"locationsCount":52},"100585739","resumption-of-enteral-feeding-after-bowel-anastomosis-100585739","NCT06906289","Resumption of Enteral Feeding After Bowel Anastomosis","Comparison of Early Versus Late Resumption of Enteral Feeding After Small Bowel Anastomosis.","Inclusion Criteria:\n\n* All patients undergoing small bowel anastomosis for any indication in elective setting\n* Patients of age between 15 to 65 years.\n* All genders\n\nExclusion Criteria:\n\n* Patient using glucocorticoids or other immunosuppressive drugs\n* non conseting individuals\n* Patient having history of gastrectomy","15 Years","65 Years",{"count":261,"type":20},204,[99],"Resumption of oral feeding after small intestine surgery is a matter of controversy .Some surgeons advocate early resumption while others don't.early feeding is initiated as soon as the patient recovers from effects of anaesthesia, while late resumption is started after 24-48 hours after surgery.Recent studies and guidelines suggest early feeding. The aim of this study is to compare the early and late resumption of oral feeding.",[35,265,266,267,268,269],"Hospital Stay, Length of Stay in Hospital From Time of Surgery Till Discharge","Defecation","Vomiting, Postoperative","Anastomotic Leak","Flatus",[271,272,273,274],"Enhanced Recover After Surgery","Hospital Stay","Postoperative vomiting","Anastomotic leak","2025-03-25",{"date":277,"type":45},"2025-04-02",{"date":279,"type":45},"2024-10-01",{"date":281,"type":20},"2025-12",{"name":283,"class":51},"Khyber Teaching Hospital",{"id":285,"slug":286,"hasResults":11,"nctId":287,"briefTitle":288,"officialTitle":289,"acronym":290,"eligibilityCriteria":291,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":292,"targetDuration":4,"studyType":64,"phases":294,"briefSummary":295,"conditions":296,"keywords":4,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":298,"lastUpdatePostDateStruct":299,"startDateStruct":301,"completionDateStruct":303,"leadSponsor":304,"locationsCount":52},"100570888","study-to-evaluate-the-impact-of-the-recovery-pathway-on-postoperative-leght-of-stay-in-coronary-artery-bypass-surgery-100570888","NCT06713096","Study to Evaluate the Impact of the Recovery Pathway on Postoperative Leght of Stay in Coronary Artery Bypass Surgery","Prospective and Randomized Study to Evaluate the Impact of the Recovery Pathway on Postoperative Leght of Stay in Coronary Artery Bypass Surgery","KAMAY","Inclusion Criteria:\n\n* Adult patients (\\>18 years old)\n* Undergoing isolated coronary artery bypass grafting (CABG) with elective or urgent status\n* Signed informed consent form (ICF)\n\nExclusion Criteria:\n\n* Emergency patients\n* Severe ventricular dysfunction (ejection fraction \\\u003C30%)\n* Renal impairment (creatinine clearance \\\u003C30 mL\u002Fmin)\n* Atrial fibrillation or need for oral anticoagulation\n* Moderate-to-severe anemia (hematocrit \\\u003C32%)\n* STS risk score \\>4%\n* Patient and\u002For family disagreement with the protocol\n* Failure to sign the informed consent form",{"count":293,"type":20},128,[99],"This randomized and prospective trial aims to evaluate the implementation of a rapid recovery protocol for coronary artery bypass grafting (CABG) in a hospital serving patients from the Brazilian Unified Health System (Sistema Único de Saúde - SUS). The study will compare outcomes between two groups: patients receiving care under the rapid recovery protocol and those following the standard institutional care.\n\nPrimary Objective:\n\nCompare postoperative hospital stay between the rapid recovery group and the usual care group.\n\nSecondary Objectives:\n\nAssess morbidity and mortality between both groups.\n\nEvaluate patient satisfaction using validated tools.\n\nAnalyze incremental costs associated with both approaches.\n\nAssess healthcare teams' learning progression regarding the protocol (Kirkpatrick method).\n\nEvaluate adherence to rapid recovery protocol metrics by healthcare teams.\n\nMeasure changes in patient safety culture among healthcare professionals.\n\nHypothesis:\n\nThe null hypothesis assumes no difference in hospital stay between the two groups. The alternative hypothesis suggests that the rapid recovery protocol will reduce hospital stay compared to the standard care. Previous findings from Mejia et al. (2022) indicated a 40% reduction in postoperative hospital stay (from 13 to 7.8 days) for cardiac surgery patients under a rapid recovery protocol at the Heart Institute (InCor HCFMUSP).\n\nThis trial will provide critical insights into the applicability of enhanced recovery after surgery (ERAS) principles in cardiac surgery within the context of public healthcare, aiming to improve outcomes and optimize resource use.",[35,297],"Quality Improvement","2024-11-26",{"date":300,"type":45},"2024-12-03",{"date":302,"type":45},"2021-11-25",{"date":281,"type":20},{"name":305,"class":51},"University of Sao Paulo General Hospital",{"id":307,"slug":308,"hasResults":11,"nctId":309,"briefTitle":310,"officialTitle":311,"acronym":312,"eligibilityCriteria":313,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":314,"targetDuration":316,"studyType":21,"phases":4,"briefSummary":317,"conditions":318,"keywords":325,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":328,"lastUpdatePostDateStruct":329,"startDateStruct":331,"completionDateStruct":333,"leadSponsor":335,"locationsCount":337},"100486389","the-fast-track-centre-for-hip-and-knee-replacement-database-100486389","NCT05613439","The Fast-track Centre for Hip and Knee Replacement Database","The Fast-track Centre for Hip and Knee Replacement Prospective Database on Preoperative Patientcharacteristics and Postoperative Complications","FCD","Inclusion Criteria:\n\n* age \\>18 years\n* non-malignant surgery\n* danish social security number\n* elective procedure\n\nExclusion Criteria:\n\n* unwilling to provide informed consent",{"count":315,"type":20},80000,"3 Months","This is a prospective study-registry on preoperative patient characteristics and postoperative complications in patients having fast-track hip and knee replacement surgery in 8 Danish dedicated arthroplasty departments from all five health regions in Denmark. The registry consists of detailed patient and physician reported preoperative characteristics and including prescribed medication and lab results. Follow-up is based on electronical medical records by dedicated nurses with physician backup and includes Clavien-Dindo and Comprehensive Complication Index scoring. All patients having day-surgery also completes a patient reported questionaire on health-care utilization and return to work by day 30. Finally, a machine-learning algorithm for identification of \"high-risk\" patients based on he preoperative data is included.",[319,320,321,35,31,322,323,324],"Hip","Knee","Fast-track Surgery","Ambulatory Surgical Procedures","Perioperative\u002FPostoperative Complications","Patient Satisfaction",[326,327,31,35,323,322],"Hip Replacement","Knee Replacement","2024-08-06",{"date":330,"type":45},"2024-08-09",{"date":332,"type":45},"2022-09-01",{"date":334,"type":20},"2027-12-31",{"name":336,"class":51},"Rigshospitalet, Denmark",8,{"id":339,"slug":340,"hasResults":11,"nctId":341,"briefTitle":342,"officialTitle":343,"acronym":4,"eligibilityCriteria":344,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":61,"enrollmentInfo":345,"targetDuration":4,"studyType":64,"phases":347,"briefSummary":348,"conditions":349,"keywords":351,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":354,"lastUpdatePostDateStruct":355,"startDateStruct":357,"completionDateStruct":359,"leadSponsor":361,"locationsCount":4},"100557697","multicentre-clinical-study-of-ultra-fast-track-anaesthesia-for-minimally-invasive-heart-valve-surgery-100557697","NCT06541483","Multicentre Clinical Study of Ultra-Fast-Track Anaesthesia for Minimally Invasive Heart Valve Surgery","A Multicenter Clinical Study of Ultra-Fast-Track Cardiac Anesthesia in Minimally Invasive Cardiac Surgery for Valvular Heart Disease","Inclusion Criteria:\n\n* Age ≥18 and ≤80 years\n* American Society of Anaesthesiologists (ASA) class I-III\n* New York Heart Association (NYHA) cardiac class III or below\n* Preoperative inspired air pulse oximetry (SpO2) ≥95%\n* Ejection fraction (EF) ≥ 40%\n* No contraindications to nerve blocks\n\nExclusion Criteria:\n\n* Patient's refusal to participate\n* Severe communication disorders\n* Severe disorders of coagulation with spontaneous bleeding tendency\n* Long-term application of opioid analgesics\n* Pulmonary hypertension (mean pulmonary artery pressure ≥55 mmHg)\n* People who need artificial ventilation\n* Allergy to dexmedetomidine and ropivacaine\n* Complex aortic root surgery such as root widening",{"count":346,"type":20},1200,[99],"The goal of this clinical trial is to evaluate the clinical effects of ultra-fast-track anesthesia (UFTA) for minimally invasive cardiac surgery (MICS) in adults. It will also learn about the safety and feasibility of Ultra-Fast-Track cardiac surgery(UFTCA).The main questions it aims to answer are:Does UFTCA promote rapid postoperative recovery, reduce postoperative complications and perioperative mortality, and improve the quality of mid- and long-term survival.And does it improve patient satisfaction and reduce healthcare costs.\n\nParticipants will receive homogenized perioperative management in the cardiac ward, extracorporeal circulation, and postoperative ICU, except for anesthesia extubation time.Furthermore，Participants need complete quality of life scales at 30 days, 90 days, six months, and one year after surgery, separately.\n\nParticipants in this study are adults who required elective minimally invasive heart valve surgery under extracorporeal circulation.This study will be able to promote rapid recovery while reducing the associated costs and the financial burden on participants.Retrospective big data analysis of perioperative clinical characteristics of patients undergoing minimally invasive heart valve surgery to establish a risk warning model and develop a perioperative management program. The investigators then conducts a randomized group trial comparing the similarities and differences between conventional general anesthesia（CGA） and ultra-fast-track cardiac anesthesia(URTCA) to demonstrate the effectiveness and safety of UFTA in MICS.Finally, building expert consensus.",[350,35],"Heart Valve Diseases",[352,353],"Ultra-fast-track Anesthesia","minimally invasive cardiac surgery","2024-08-02",{"date":356,"type":45},"2024-08-07",{"date":358,"type":20},"2024-12",{"date":360,"type":20},"2028-12",{"name":362,"class":51},"Zhejiang Provincial People's Hospital",{"id":364,"slug":365,"hasResults":11,"nctId":366,"briefTitle":367,"officialTitle":368,"acronym":4,"eligibilityCriteria":369,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":259,"enrollmentInfo":370,"targetDuration":4,"studyType":64,"phases":372,"briefSummary":373,"conditions":374,"keywords":375,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":377,"lastUpdatePostDateStruct":378,"startDateStruct":380,"completionDateStruct":382,"leadSponsor":384,"locationsCount":52},"100406754","patients-undergoing-laparoscopic-colorectal-surgery-walk-out-from-operating-room-after-surgery--wofor-c1--100406754","NCT04576533","Patients Undergoing Laparoscopic Colorectal Surgery Walk Out From Operating Room After Surgery ( WOFOR-C1 )","Effects of Walking Out From Operating Room on Postoperative Recovery of Patients Undergoing Laparoscopic Colorectal Surgery","Inclusion Criteria:\n\n* 1\\. Age 18-65 Years old\n* 2\\. scheduled for laparoscopic colectomy or laparoscopic rectectomy surgery (Dixon technique)\n* 3\\. American Society of anesthesiology (ASA) grade I or grade II\n\nExclusion Criteria:\n\n* 1\\. Patients have severe cardiac diseases (cardiac function grading greater than grade 3\u002Farrhythmia including sick sinus syndrome, atrial fibrillation, atrial flutter, atrioventricular block, frequent ventricular premature, multiple ventricular premature, ventricular premature R on T, ventricular fibrillation and ventricular flutter\u002Facute coronary syndrome) or respiratory failure or hepatic failure or renal failure;\n* 2\\. Patients with poor blood glucose control (glycosylated hemoglobin\\>7%);\n* 3\\. Patients with poor blood pressure control (receive regular antihypertensive medical treatment but still have systolic blood pressure \\> 150 mmHg and\u002For diastolic blood pressure \\> 90 mmHg );\n* 4\\. Patients have schizophrenia, epilepsy, Parkinson's disease, mental retardation, or hearing impairment.\n* 5\\. Patients have thrombosis such as in lower extremity or in other veins.\n* 6\\. Patients have neuromuscular disorders affecting lower limb activity, such as myasthenia gravis and cerebral infarction, which cause lower limb muscle weakness;\n* 7\\. Patients have contraindications for epidural puncture.\n* 8\\. Patients refuse to sign informed consent for research.",{"count":371,"type":20},300,[99],"Early mobilization is considered as an important strategy to enhance postoperative recovery. However, direct association between very early mobilization and improved recovery needs randomized control trials to prove. This study proposes the program of walking out from operating room (WOFOR) after surgery, which means that encouraging patients to walk out from the operating room and return to the ward by walking under the condition of painlessness, clear consciousness and normal muscle strength of lower limb. The aim of this randomized controlled trial is to investigate the effect of WOFOR on the postoperative recovery of patients undergoing laparoscopic colorectal surgery.",[35],[376],"early mobilization","2024-07-05",{"date":379,"type":45},"2024-07-08",{"date":381,"type":45},"2020-11-01",{"date":383,"type":20},"2025-12-01",{"name":385,"class":51},"Sixth Affiliated Hospital, Sun Yat-sen University",{"id":387,"slug":388,"hasResults":11,"nctId":389,"briefTitle":390,"officialTitle":391,"acronym":4,"eligibilityCriteria":392,"healthyVolunteers":125,"sex":16,"minAge":17,"maxAge":393,"enrollmentInfo":394,"targetDuration":4,"studyType":64,"phases":396,"briefSummary":397,"conditions":398,"keywords":4,"overallStatus":108,"whyStopped":4,"lastUpdateSubmitDate":399,"lastUpdatePostDateStruct":400,"startDateStruct":402,"completionDateStruct":404,"leadSponsor":405,"locationsCount":52},"100479861","self-reported-outcomes-of-patients-in-eras-nursing-100479861","NCT05528484","Self-reported Outcomes of Patients in ERAS Nursing","Effect of ERAS Nursing on Self-reported Outcomes of Patients Undergoing Minimally Invasive Lung Cancer Surgery","Inclusion Criteria:\n\n* ≥18years,Minimally invasive elective surgery,cooperate\n\nExclusion Criteria:\n\n* Pneumonectomy was performed and converted to open surgery\n\nSurgery intensive care, unable to cooperate (language\n\nSpeech disorders, psychopathology)","85 Years",{"count":395,"type":20},600,[99],"We aimed to evaluate the effect of ERAS nursing program on self-reported outcomes of patients undergoing minimally invasive lung cancer surgery, and compared the differences in length of hospital stay, complications, and readmission rate between ERAS and non-ERAS nursing programs",[35],"2022-11-14",{"date":401,"type":45},"2022-11-16",{"date":403,"type":45},"2019-10-01",{"date":114,"type":20},{"name":406,"class":51},"The Second Hospital of Shandong University"]