[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"abdominal-surgeries\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:abdominal-surgeries":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,6,0,[8,50,76,102,129,180],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":33,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100621465","effect-of-clinical-hypnosis-in-preoperative-anxiety-among-patients-undergoing-an-abdominal-surgery-100621465",false,"NCT07370974","Effect of Clinical Hypnosis in Preoperative Anxiety Among Patients Undergoing an Abdominal Surgery.","Effect of Clinical Hypnosis in Preoperative Anxiety Among Patients Undergoing an Abdominal Surgery : a Multicenter Randomized Controlled Trial.","Hypnoanxiety","* Inclusion Criteria:\n\n  1. Consenting patients undergoing abdominal surgery\n  2. ASA I-II physical status\n  3. Able to understand and respond to instructions\n  4. No major psychological disorders\n* Exclusion Criteria:\n\n  1. Non-consenting patients\n  2. Prior experience with hypnosis\n  3. History of mental illness\n  4. Psychoactive substance consumption\n  5. Cognitive disorders","ALL","18 Years","80 Years",{"count":21,"type":22},48,"ESTIMATED","INTERVENTIONAL",[25],"NA","This Multicenter randomized controlled trial evaluates clinical hypnosis efficacy for reducing perioperative anxiety and postoperative pain in abdominal surgery patients across 3 Moroccan centers (n=48-68). Intervention arm receives 15-20 min level 2 hypnosis session preoperatively; control receives standard psychological preparation. Primary outcome: VAS-anxiety post-intervention. Secondary: postoperative EVA-pain, analgesic consumption, length of stay.\n\nStudy Design Prospective, multicenter, parallel-group RCT (1:1 allocation, stratified by center\u002Fsex). Inclusion: consenting ASA I-II adults for abdominal surgery. Primary endpoint powered for 10mm EVA reduction (80% power, α=0.05). Registration supports PhD thesis at ISSS\u002FUniversité Hassan 1er Settat.",[28,29,30,31,32],"Hypnosis","Preoperative Anxiety","Postoperative Pain","Abdominal Surgeries","Length of Stay",[34,35,28,36],"RCT","Morocco","preoperative anxiety","RECRUITING","2026-05-30",{"date":40,"type":41},"2026-06-02","ACTUAL",{"date":43,"type":41},"2026-02-07",{"date":45,"type":22},"2026-06-03",{"name":47,"class":48},"HASSAN 1st university","OTHER",3,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":58,"maxAge":4,"enrollmentInfo":59,"targetDuration":4,"studyType":61,"phases":4,"briefSummary":62,"conditions":63,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100623298","can-ultrasound-guided-fascial-plane-blocks-reduce-postoperative-pulmonary-complications-after-major-abdominal-surgery-100623298","NCT07394816","Can Ultrasound-Guided Fascial Plane Blocks Reduce Postoperative Pulmonary Complications After Major Abdominal Surgery?","The Effect of Ultrasound-Guided Fascial Plane Blocks on Postoperative Pulmonary Complications in Patients Undergoing Major Abdominal Surgery: A Prospective Observational Study","FPB-PPC","Inclusion Criteria:\n\n* Age 65 years or older\n* Scheduled for elective major abdominal surgery (e.g., colorectal, hepatobiliary, pancreatic, or gastric surgery)\n* ASA physical status II-III\n* Ability to provide written informed consent\n* Planned use of general anesthesia with or without adjunct regional techniques\n\nExclusion Criteria:\n\n* Refusal or inability to provide informed consent\n* Known allergy or contraindication to local anesthetics\n* Coagulopathy or ongoing anticoagulant therapy contraindicating regional anesthesia\n* Infection at the site of planned block\n* Pre-existing chronic opioid use or chronic pain syndrome\n* Severe hepatic, renal, or cardiac failure (e.g., Child-Pugh C, end-stage renal disease, EF \\\u003C30%)\n* Cognitive impairment or severe dementia preventing adequate pain assessment\n* Emergency surgery\n* Body mass index (BMI \\> 40 kg\u002Fm²)","65 Years",{"count":60,"type":22},500,"OBSERVATIONAL","This prospective observational study aims to evaluate whether the use of ultrasound-guided fascial plane blocks is associated with a lower incidence of postoperative pulmonary complications in adult patients undergoing elective major abdominal surgery under general anesthesia.\n\nPatients will be observed in two groups based on routine clinical practice: those who receive an ultrasound-guided fascial plane block for postoperative analgesia and those managed with other standard analgesic methods. The choice of analgesic technique will be determined by the responsible anesthesia team and not influenced by the study.\n\nPostoperative pulmonary complications occurring within the first 7 days after surgery will be recorded using reopening the European Perioperative Clinical Outcome (EPCO) criteria. Secondary outcomes will include unplanned intensive care unit admission, length of hospital stay, and 30-day mortality. No additional procedures or interventions will be performed for research purposes.",[64,31,65],"Postoperative Pulmonary Complications (PPCs)","Postoperative Pain Management","2026-04-25",{"date":68,"type":41},"2026-04-30",{"date":70,"type":41},"2026-03-01",{"date":72,"type":22},"2026-08-15",{"name":74,"class":48},"Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital",1,{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":17,"minAge":83,"maxAge":84,"enrollmentInfo":85,"targetDuration":4,"studyType":23,"phases":87,"briefSummary":88,"conditions":89,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":75},"100601404","nalbuphine-versus-tramadol-on-post-operative-analgesia-in-abdominal-surgery-on-pediatric-cancer-patient-100601404","NCT07110051","Nalbuphine Versus Tramadol on Post Operative Analgesia in Abdominal Surgery on Pediatric Cancer Patient","Comparative Study Between Nalbuphine Versus Tramadol on Post Operative Analgesia in Abdominal Surgery on Pediatric Cancer Patient","Inclusion Criteria:\n\n* Participants will be children aged 3-12 years\n* American society of anesthesia (ASA) classification I-III.\n* scheduled for elective Abdominal surgery under general anesthesia\n\nExclusion Criteria:\n\n* child guardian refusal.\n* Allergy from Tramal or nalbuphine\n* Patient with previous chronic pain on opioids","3 Years","12 Years",{"count":86,"type":22},128,[25],"In current study the investigators aim to compare between nalbuphine versus tramadol for post-operative pain control in abdominal surgeries in pediatric.",[90,91,31,92],"Tramadol","Nalbuphine","Pediatric Cancer","2025-08-06",{"date":95,"type":41},"2025-08-11",{"date":97,"type":41},"2025-01-15",{"date":99,"type":22},"2025-10-15",{"name":101,"class":48},"National Cancer Institute, Egypt",{"id":103,"slug":104,"hasResults":11,"nctId":105,"briefTitle":106,"officialTitle":107,"acronym":4,"eligibilityCriteria":108,"healthyVolunteers":11,"sex":17,"minAge":58,"maxAge":4,"enrollmentInfo":109,"targetDuration":4,"studyType":23,"phases":111,"briefSummary":112,"conditions":113,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":75},"100601305","intraoperative-infusion-of-either-lidocaine-or-dexmedetomidine-on-regional-cerebral-oxygen-saturation-and-postoperative-delirium-in-elderly-patients-undergoing-abdominal-surgeries-100601305","NCT07108764","Intraoperative Infusion of Either Lidocaine or Dexmedetomidine on Regional Cerebral Oxygen Saturation and Postoperative Delirium in Elderly Patients Undergoing Abdominal Surgeries","Effect of Intraoperative Infusion of Either Lidocaine or Dexmedetomidine on Regional Cerebral Oxygen Saturation and Postoperative Delirium in Elderly Patients Undergoing Abdominal Surgeries","Inclusion Criteria:\n\n* Age ≥ 65years old.\n* Both sexes.\n* Physical status classification of II - III according to the American Society of Anesthesiologists (ASA).\n* Undergo elective non-cardiac surgeries.\n\nExclusion Criteria:\n\n* History of mental illness, neurological illness, or scoring less than 8 using the abbreviated mental test (AMT) before operation.\n* Severe hearing or visual impairment that may interfere with communication.\n* Severe renal or hepatic dysfunction.\n* Patients on central nervous system (CNS) medications (antipsychotics, anticonvulsants, antiparkinsonian, antidepressants).\n* Contraindications to lidocaine or dexmedetomidine \\[e.g., allergy, severe bradycardia, atrioventricular (AV) block\\].",{"count":110,"type":22},100,[25],"This study aims to compare the effect of intraoperative infusion of either lidocaine or dexmedetomidine on the incidence of postoperative delirium (POD) in elderly patients undergoing major surgeries. It also aims to evaluate the impact of both medications on intraoperative regional cerebral oxygen saturation (rSO₂).",[114,115,116,117,118,119,31],"Intraoperative Infusion","Lidocaine","Dexmedetomidine","Cerebral Oxygen Saturation","Postoperative Delirium","Elderly Patients","2025-07-31",{"date":122,"type":41},"2025-08-07",{"date":124,"type":41},"2025-04-17",{"date":126,"type":22},"2027-04-01",{"name":128,"class":48},"Tanta University",{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":135,"eligibilityCriteria":136,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":137,"targetDuration":4,"studyType":23,"phases":139,"briefSummary":141,"conditions":142,"keywords":152,"overallStatus":170,"whyStopped":4,"lastUpdateSubmitDate":171,"lastUpdatePostDateStruct":172,"startDateStruct":174,"completionDateStruct":176,"leadSponsor":178,"locationsCount":75},"100587065","phase-4-intravenous-acetaminophen-to-reduce-post-operative-opioid-consumption-100587065","NCT06923540","Intravenous Acetaminophen to Reduce Post-operative Opioid Consumption","Evaluating the Impact of IV Acetaminophen on Opioid Consumption in the Postoperative Period in Patients Undergoing Abdominal Surgery","ACETAPOP","Inclusion Criteria:\n\n* Age 18 years or older.\n* Underwent abdominal surgery\n* Underwent elective surgery.\n* Hospitalized in the digestive surgery, hepatobiliary and pancreatic surgery, or gynecology and gynecologic oncology units at CHUM.\n* Declared NPO immediately post-surgery, meaning they cannot take oral medications.\n\nExclusion Criteria:\n\n* Hypersensitivity to acetaminophen or an excipient in the administered formulations\n* Hepatic insufficiency with a Child-Turcotte-Pugh score of B or C.\n* Weight \\\u003C 50 kg (patients requiring a lower acetaminophen dose).\n* Active pregnancy or breastfeeding.\n* Opioid use disorder (OUD) under active treatment\n* Non-opioid-naïve patients: those who received a long-acting opioid within seven days preceding surgery. This criterion will be verified through patient interviews and cross-checked with medical records.\n* Use of illicit recreational substances.\n* Prior participation in this study.\n* Ectopic patients: physically located in a unit other than digestive surgery (11 South), hepatobiliary and pancreatic surgery (14 South), or gynecology and gynecologic oncology (12 South).",{"count":138,"type":22},140,[140],"PHASE4","Acetaminophen (Tylenol) is a commonly used medication after surgery to control pain. Tablets for oral use and suppositories for rectal use are the most frequently employed forms of acetaminophen after surgery. Intravenous (IV) acetaminophen is widely used in several countries but is not a standard medication for the adult population in Canada. It is mainly considered when it is impossible to take medication in tablet or suppository form. Opioids (Morphine, Hydromorphone, Oxycodone, etc.) are another class of medications commonly used after surgery for pain management. While they are generally very effective and stronger than acetaminophen or other pain relievers (e.g., ibuprofen\u002FAdvil), reducing their use is preferable, as they can cause various side effects such as nausea, dizziness, and dependence. IV acetaminophen may help control pain while also reducing opioid consumption. However, there are few high-quality scientific studies proving the benefits of IV acetaminophen compared to other forms, such as tablets or suppositories. Acetaminophen has been available in Canada for many years and has already been recommended for use in Quebec by the Institut national d'excellence en santé et services sociaux (INESSS) under certain conditions. This study aims to validate its benefits with clear data.",[143,144,145,31,146,147,148,149,150,32,151],"Post Operative Analgesia","Opioid Consumption, Postoperative","Acetaminophen","Post Operative Bowel Dysfunction","Post Operative Nausea and Vomiting","Post Operative Pain Control","Mobility","Epidural Analgesia","Pain Management",[153,154,155,156,157,158,159,160,161,162,163,164,165,166,167,168,169],"IV acetaminophen","intravenous acetaminophen","acetaminophen","post operative analgesia","nil per os","npo","post operative pain","opioid consumption","abdominal surgery","hepato-biliary surgery","digestive surgery","pancreatic surgery","gynecologic surgery","post operative nausea and vomiting","post operative mobility","hospitalization length of stay","co-analgesia","NOT_YET_RECRUITING","2025-04-04",{"date":173,"type":41},"2025-04-11",{"date":175,"type":22},"2025-04-28",{"date":177,"type":22},"2025-08-15",{"name":179,"class":48},"Centre hospitalier de l'Université de Montréal (CHUM)",{"id":181,"slug":182,"hasResults":11,"nctId":183,"briefTitle":184,"officialTitle":184,"acronym":4,"eligibilityCriteria":185,"healthyVolunteers":186,"sex":17,"minAge":187,"maxAge":188,"enrollmentInfo":189,"targetDuration":191,"studyType":61,"phases":4,"briefSummary":192,"conditions":193,"keywords":197,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":202,"lastUpdatePostDateStruct":203,"startDateStruct":205,"completionDateStruct":207,"leadSponsor":209,"locationsCount":75},"100577278","validity-and-reliability-of-the-arabic-version-of-de-morton-mobility-index-after-abdominal-surgeries-100577278","NCT06796218","Validity and Reliability of the Arabic Version of De Morton Mobility Index After Abdominal Surgeries","Inclusion Criteria:\n\n1. Patients after abdominal surgeries.\n2. Patients aged between 40 and 60 years.\n3. All patients are able to read and write in Arabic language.\n4. All patients can understand items of the scale.\n5. All patients will follow the given instructions during the assessment\n\nExclusion Criteria:\n\n1. Patients with mental disabilities .\n2. Patients with communication, vision and hearing disorders\n3. Patients who are not co-operative .\n4. patients who are contraindicated to mobilize due to medical reasons.\n5. patients who are isolated due to infection.",true,"40 Years","60 Years",{"count":190,"type":22},103,"2 Days","PURPOSE: To determine validity and reliability of translated Arabic version of the De Morton Mobility index for mobility assessment in patients after abdominal surgeries.\n\nBACKGROUND:\n\nMajor abdominal surgery has a high morbidity and Mortality rate, and the risk of surgical complications is higher than for equivalent elective operations. those receiving emergency laparotomy are in a condition of physiological derangement driven by inflammation that has already occurred prior to surgery, in contrast to those undergoing elective abdominal operations. early mobility and exercise play an important role in postoperative treatment following abdominal surgery and are related with reduced postoperative fitness loss and fewer postoperative complications in individuals undergoing elective surgery. reduced mobility is a primary factor of lower quality of life and decreased social participation. reduced mobility is particularly common in older hospitalized patients, and it leads to an increased risk of falls, longer hospitalizations, more severe impairment and morbidity, and higher mortality rates. To manage elderly patients' mobility function, a reliable and valid mobility assessment tool is required. Performance-based examinations are commonly used to measure the mobility of elderly individuals. The De Morton Mobility Index (DEMMI) was established and validated exclusively for older patients hospitalized in the ward. The DEMMI provides clinicians and researchers with a valid interval-level method for accurately measuring and monitoring mobility levels of acute medical patients. It has been validated also in sub acute hospital and community settings. A DEMMI score of \\\u003C40 indicates an independent risk of serious postoperative complications. A low DEMMI score suggested impaired mobilization, and prior research of patients following abdominal surgery discovered that delayed mobilization was related with postoperative pulmonary complications.\n\nHYPOTHESES: It will be hypothesized that: Arabic version of the De Morton Mobility Index may be valid and reliable in patients after abdominal surgeries.\n\nRESEARCH QUESTION: Is The Arabic version of the De Morton Mobility index valid and reliable for mobility assessment in patients after abdominal surgeries?",[31,194,195,196],"Mobility Limitation","Mobility Difficulty","Abdominal Surgery Patients",[198,199,200,201],"mobility limitation","mobility difficulty","abdominal surgeries","abdominal surgical approaches","2025-01-26",{"date":204,"type":41},"2025-01-28",{"date":206,"type":41},"2024-09-01",{"date":208,"type":22},"2025-01-30",{"name":210,"class":48},"Cairo University"]