[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"abdominal-surgery-complications\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:abdominal-surgery-complications":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,54,81],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":33,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":4},"100643245","prehabilitation-in-high-risk-oncologic-surgery-100643245",false,"NCT07638410","Prehabilitation in High-risk Oncologic Surgery","SURG-236: Prehabilitation in High-risk Oncologic Surgery: A Prospective Cohort Study","Inclusion Criteria:\n\n* Evidence of probable or confirmed primary or recurrent malignant neoplasm of any stage\n* Planned to undergo neoadjuvant chemotherapy or chemoradiation\n* Eligible surgical candidate for one of the following procedures: pancreatectomy, gastrectomy, esophagectomy, cystectomy, low anterior resection, abdominoperineal resection, or cytoreductive surgery with heated intraperitoneal chemotherapy\n* Age greater than 18 years\n* Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2\n* Ability to understand and willingness to sign a written informed consent form and Health Insurance Portability and Accountability Act (HIPAA) authorization document\n\nExclusion Criteria:\n\n* Unable to complete study requirements, such as attending a minimum of two visits for each specialty referral. This will be assessed at the final preoperative visit, at which time the participant may be discontinued from the study and replaced. Participants will not be excluded due to lack of insurance coverage for health psychology visits.\n* Does not proceed to surgery at an affiliated institution\n* Pregnant or breastfeeding","ALL","18 Years",{"count":19,"type":20},180,"ESTIMATED","INTERVENTIONAL",[23],"NA","The goal of this clinical study is to learn whether a prehabilitation program can improve recovery after major abdominal surgery in adults with cancer who are receiving treatment before surgery. Prehabilitation is supportive care given before surgery to help patients prepare physically, nutritionally, and emotionally.\n\nThe main questions this study aims to answer are:\n\n1. Does prehabilitation reduce the number of participants who die or have serious complications within 30 days after surgery?\n2. Does prehabilitation improve physical strength and fitness, nutritional status, emotional well-being, and quality of life before surgery?\n3. Does prehabilitation affect the length of the hospital stay after surgery, the time it takes to start additional cancer treatment after surgery, or the ability to complete recommended additional treatment?\n\nParticipants will take part in a prehabilitation program during their treatment period before surgery. The program includes visits with physical therapy, nutrition, and health psychology. Participants will meet with each specialty at least twice before surgery. They will also complete questionnaires and tests that measure physical function, diet and weight, emotional well-being, and quality of life. After surgery, information about recovery and additional cancer treatment will be collected from medical records for up to 120 days.\n\nResearchers will compare the outcomes of participants who receive the prehabilitation program with outcomes from similar patients who previously received care at Fox Chase Cancer Center but did not participate in this study.",[26,27,28,29,30,31,32],"Pancreatic Cancer","Colo-rectal Cancer","Gastric Cancer","Esophageal Cancer","Bladder Cancer","Ovarian Cancer","Abdominal Surgery Complications",[34,35,36,37,38,39,40,41],"Prehabilitation","Preoperative Rehabilitation","Multimodal Prehabilitation","Major Abdominal Surgery","Oncologic Surgery","Neoadjuvant Therapy","Postoperative Complications","Cancer Surgery","NOT_YET_RECRUITING","2026-06-09",{"date":45,"type":46},"2026-06-11","ACTUAL",{"date":48,"type":20},"2026-06-15",{"date":50,"type":20},"2030-03-15",{"name":52,"class":53},"Fox Chase Cancer Center","OTHER",{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":4,"eligibilityCriteria":59,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":21,"phases":62,"briefSummary":63,"conditions":64,"keywords":66,"overallStatus":70,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":80},"100603486","the-effect-of-heating-the-intensive-care-room-in-the-early-postoperative-period-on-patient-outcomes-100603486","NCT07137143","The Effect of Heating the Intensive Care Room in the Early Postoperative Period on Patient Outcomes","Inclusion Criteria:\n\n* The following criteria will be included in the sample:\n* Patients who underwent elective abdominal surgery and were admitted to intensive care after surgery.\n* Patients aged 18 and over.\n* Patients whose body temperature on the morning of surgery was neither below 36°C nor above 37.5°C.\n* Patients who did not have a pacemaker, dementia, advanced spasticity, muscle atrophy, peripheral lesions, osteoporosis, skin irritation, diabetes, hypertension, or obesity.\n* Patients who did not require mechanical ventilation.\n* Patients who did not have any illness that would impair thermoregulation (such as head trauma or hypothalamic damage).\n\n  • Patients who were not taking medications that would affect thermoregulation, such as vasodilators.\n* Patients who did not have peripheral circulation problems.\n* Patients who were not alcohol or substance abusers.\n* Patients who did not have mental retardation.\n* Patients who were conscious and oriented to person, time, and place.\n* Patients who could speak Turkish.\n* Patients who did not have any auditory or visual impairments.\n* Patients who volunteered for the study.\n\nExclusion Criteria:\n\n* Patients who do not meet the sampling criteria, who develop postoperative complications (bleeding, intubation, stenosis, necrosis, ileus, dermatitis, parastomal herniation, etc.), and whose relatives do not consent to the study will not be included in the study.",{"count":61,"type":20},70,[23],"The aim of this study was to evaluate the effect of heating the intensive care room in the early postoperative period on patient outcomes.",[32,65],"Hypothermia Following Anesthesia",[67,68,69],"intensive care unit","hypothermia","postoperative warming","RECRUITING","2025-08-26",{"date":73,"type":46},"2025-08-27",{"date":75,"type":46},"2025-04-20",{"date":77,"type":20},"2025-10-30",{"name":79,"class":53},"Cukurova University",1,{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":86,"acronym":87,"eligibilityCriteria":88,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":89,"targetDuration":91,"studyType":92,"phases":4,"briefSummary":93,"conditions":94,"keywords":98,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":112,"completionDateStruct":114,"leadSponsor":116,"locationsCount":4},"100599014","adhesion-prevention-in-asbo-surgery-using-4dryfield-ph-100599014","NCT07078981","Adhesion Prevention in ASBO Surgery Using 4DryField® PH","Assessing Determinants of Headway in Evaluating Risk of Adhesion: the ADHERE Study","ADHERE","Inclusion Criteria:\n\nAge ≥ 18 years\n\n* Undergoing surgical treatment for adhesive small bowel obstruction (ASBO)\n* Ability and willingness to provide informed consent\n* Willingness to adhere to follow-up visits\n\nExclusion Criteria:\n\n* Presence of peritonitis\n* Intra-abdominal active malignancy\n* Pregnancy or breastfeeding",{"count":90,"type":20},189,"1 Year","OBSERVATIONAL","Post-surgical adhesions occur in up to 90% of abdominal surgeries, often leading to complications like adhesive small bowel obstruction (ASBO) and chronic pain. They result from imbalanced healing processes influenced by growth factors, fibroblast activity, and genetic predispositions. While surgery can relieve ASBO, it frequently causes new adhesions, with recurrence rates up to 40%. Anti-adhesion barriers, such as the starch-based 4DryField® PH, form a temporary gel barrier to support healing. Though promising, its role in preventing ASBO recurrence is not well studied. This study evaluates whether intra-operative use of 4DryField® PH reduces ASBO recurrence over 12 months and compares perioperative outcomes in treated vs. untreated patients.",[95,96,97,32],"Adhesive Small Bowel Obstruction","Postoperative Abdominal Adhesions","Bowel Obstruction",[99,100,101,102,103,104,105,106,107,108],"adhesion","obstruction","acute abdomen","emergency surgery","4DryField","adhesiolysis","antiadhesion barrier","ASBO","abdominal surgery","peritoneal adhesion","2025-07-14",{"date":111,"type":46},"2025-07-22",{"date":113,"type":20},"2025-07-15",{"date":115,"type":20},"2027-07-15",{"name":117,"class":53},"Alessio Giordano"]