[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"abdominal-cancer-surgery\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:abdominal-cancer-surgery":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,50],{"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":31,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100648355","developing-pilot-postoperative-guidelines-for-improved-functional-outcomes-after-high-risk-cancer-surgery-100648355",false,"NCT07720089","Developing Pilot Postoperative Guidelines for Improved Functional Outcomes After High-Risk Cancer Surgery","Development and Implementation of Pilot Postoperative Guidelines to Improve Functional Outcomes Following High-Risk Surgery for Cancer: A North American Prospective Feasibility Study","Inclusion Criteria:\n\n* Surgeons who perform abdominal surgery for cancer at the study institution\n\nExclusion Criteria:\n\n* Surgeons who do not perform abdominal surgery for cancer\n* Surgeons who are external to the study institution","ALL","18 Years",{"count":19,"type":20},66,"ESTIMATED","INTERVENTIONAL",[23],"NA","The objective of this study is to develop and evaluate the implementation of novel timeline-specific National Comprehensive Cancer Network (NCCN)-style clinical guidelines designed to improve functional outcomes after high-risk abdominal surgery for cancer.",[26,27,28,29,30],"Cancer","Abdominal Cancer Surgery","Surgery","Recovery Outcomes","Functional Outcomes",[32,33,34,35,36],"cancer","abdominal cancer surgery","surgery","recovery outcomes","functional outcomes","NOT_YET_RECRUITING","2026-07-31",{"date":40,"type":41},"2026-08-03","ACTUAL",{"date":43,"type":20},"2026-07",{"date":45,"type":20},"2027-08",{"name":47,"class":48},"University of Alabama at Birmingham","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":56,"targetDuration":4,"studyType":21,"phases":58,"briefSummary":60,"conditions":61,"keywords":62,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":4},"100569532","phase-4-efficacy-and-safety-of-adding-dexmedetomidine-to-levobupivacaine-in-rectus-sheath-block-compared-to-quadratus-lumborum-block-in-patients-undergoing-lower-abdominal-cancer-surgery-a-randomized-clinical-trial-100569532","NCT06695468","Efficacy and Safety of Adding Dexmedetomidine to Levobupivacaine in Rectus Sheath Block Compared to Quadratus Lumborum Block in Patients Undergoing Lower Abdominal Cancer Surgery: A Randomized Clinical Trial","Inclusion Criteria:\n\n1. Patients subjected to major lower abdominal cancer surgeries.\n2. The enrolled age will be from 18 years to 70 years\n3. ASA I-III and NYHA I-III.\n\nExclusion Criteria:\n\n1. ASA physical status \\>III and NYHA\\>III\n2. Patient refusal\n3. Body mass index \\>40 kg\u002Fm2\n4. Preoperative opioid consumption\n5. Infection at the incision site\n6. A history of hematological disorders or coagulation abnormality\n7. Previous abdominal surgeries, severe hepatic or renal impairment\n8. Pregnant women\n\n10- Hypersensitivity to any of used drugs",{"count":57,"type":20},122,[59],"PHASE4","Surgical trauma activates numerous receptors leading to severe postoperative pain. Seventy to seventy-five percent of the pain is somatic, originating from the anterior abdominal wall, and it often persists for 72 hours after open surgery. The objective of this study is to compare the efficacy and safety of adding dexmedetomidine to Levobupivacaine in rectus sheath block with quadrates lumborum block in patients undergoing lower abdominal cancer surgeries.",[27],[63,64,65,66],"Quadratus Lumborum Block","dexmedetomidine","Levobupivacaine","Rectus sheath block","2024-11-17",{"date":69,"type":41},"2024-11-19",{"date":71,"type":20},"2024-12-01",{"date":73,"type":20},"2027-01-01",{"name":75,"class":48},"Assiut University"]