{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Intestinal+Anastomosis+Complication", "query": { "condition": "Intestinal Anastomosis Complication" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 13, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Intestinal+Anastomosis+Complication&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-07-23T23:05:58.309Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT00557349", "title": "Ulcer Prevention Study in Post Gastric Bypass Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Marginal Ulcers" ], "interventions": [ { "name": "Omeprazole", "type": "DRUG" }, { "name": "Famotidine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Missouri-Columbia", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 40, "start_date": "2006-11", "completion_date": "2008-03", "has_results": true, "last_update_posted_date": "2017-01-19", "last_synced_at": "2026-07-23T23:05:58.309Z", "location_count": 1, "location_summary": "Columbia, Missouri", "locations": [ { "city": "Columbia", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT00557349" }, { "nct_id": "NCT04066894", "title": "Sacral Nerve Stimulation in Treating Low Anterior Resection Syndrome or Fecal Incontinence in Patients With Locally Advanced Rectal Cancer or Other Pelvic Cancer, the RESTORE Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Low Anterior Resection Syndrome", "Malignant Anal Neoplasm", "Malignant Bladder Neoplasm", "Malignant Cervical Neoplasm", "Malignant Ovarian Neoplasm", "Malignant Pelvic Neoplasm", "Malignant Prostate Neoplasm", "Malignant Uterine Neoplasm", "Malignant Vaginal Neoplasm", "Malignant Vulvar Neoplasm", "Rectal Carcinoma" ], "interventions": [ { "name": "Explantation", "type": "PROCEDURE" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Sacral Nerve Stimulator", "type": "DEVICE" }, { "name": "Sacral Nerve Stimulator Battery", "type": "DEVICE" }, { "name": "Therapeutic Conventional Surgery", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "OTHER", "DEVICE" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 3, "start_date": "2019-04-12", "completion_date": "2022-09-01", "has_results": true, "last_update_posted_date": "2023-08-14", "last_synced_at": "2026-07-23T23:05:58.309Z", "location_count": 2, "location_summary": "Houston, Texas • Sugar Land, Texas", "locations": [ { "city": "Houston", "state": "Texas" }, { "city": "Sugar Land", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04066894" }, { "nct_id": "NCT02178228", "title": "Observational Analysis of the Cause of Leaks When Bowel is Cut and Reconnected", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Anastomotic Leaks" ], "interventions": [], "intervention_types": [], "sponsor": "Icahn School of Medicine at Mount Sinai", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "15 Years", "maximum_age": null, "sex": "ALL", "summary": "15 Years and older" }, "enrollment_count": 1077, "start_date": "2013-10", "completion_date": "2018-01-31", "has_results": false, "last_update_posted_date": "2018-02-05", "last_synced_at": "2026-07-23T23:05:58.309Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02178228" }, { "nct_id": "NCT01301417", "title": "Data Collection of Patients Treated With the ColonRing™ for the Creation of Circular Compression Anastomosis", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Diverticulum, Colon", "Colorectal Neoplasms", "Crohn Disease", "Colitis, Ulcerative", "Colostomy", "Ileostomy - Stoma", "Rectal Prolapse", "Intestinal Polyposis", "Lymphoma", "Endometriosis", "Intestinal Volvulus" ], "interventions": [ { "name": "ColonRing™", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "novoGI", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 171, "start_date": "2011-02", "completion_date": "2011-08", "has_results": false, "last_update_posted_date": "2013-06-05", "last_synced_at": "2026-07-23T23:05:58.309Z", "location_count": 1, "location_summary": "Riverdale, Georgia", "locations": [ { "city": "Riverdale", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01301417" }, { "nct_id": "NCT05826743", "title": "Safety and Effectiveness Evaluation of the COLO-BT as an Alternative Treatment to the Ileostomy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Colorectal Surgery", "Colorectal Cancer", "Rectal/Anal", "Ileostomy - Stoma", "Anastomotic Leakage" ], "interventions": [ { "name": "COLO BT™", "type": "DEVICE" }, { "name": "Stoma Creation", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "JSR Medical Co., Ltd.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "19 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "19 Years to 80 Years" }, "enrollment_count": 256, "start_date": "2023-12-04", "completion_date": "2027-03-15", "has_results": false, "last_update_posted_date": "2025-06-13", "last_synced_at": "2026-07-23T23:05:58.309Z", "location_count": 3, "location_summary": "Buffalo, New York • Hershey, Pennsylvania • Houston, Texas", "locations": [ { "city": "Buffalo", "state": "New York" }, { "city": "Hershey", "state": "Pennsylvania" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05826743" }, { "nct_id": "NCT03952195", "title": "Complications and Outcomes of Pouch Excision", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Ulcerative Colitis", "Inflammatory Bowel Diseases" ], "interventions": [], "intervention_types": [], "sponsor": "Icahn School of Medicine at Mount Sinai", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 94, "start_date": "2015-11-01", "completion_date": "2018-04-01", "has_results": false, "last_update_posted_date": "2019-05-16", "last_synced_at": "2026-07-23T23:05:58.309Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03952195" }, { "nct_id": "NCT01880918", "title": "A RETROspective Data Collection of comPRESSion Anastomosis Using the ColonRing", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Diverticulum, Colon", "Colorectal Neoplasms", "Crohn Disease", "Colitis, Ulcerative", "Colostomy", "Ileostomy - Stoma", "Rectal Prolapse", "Intestinal Polyposis", "Lymphoma", "Endometriosis", "Intestinal Volvulus" ], "interventions": [], "intervention_types": [], "sponsor": "novoGI", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 200, "start_date": "2012-10", "completion_date": "2013-07", "has_results": false, "last_update_posted_date": "2013-06-19", "last_synced_at": "2026-07-23T23:05:58.309Z", "location_count": 3, "location_summary": "Atlamonte Springs, Florida • Port Charlotte, Florida • Springfield, Missouri", "locations": [ { "city": "Atlamonte Springs", "state": "Florida" }, { "city": "Port Charlotte", "state": "Florida" }, { "city": "Springfield", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT01880918" }, { "nct_id": "NCT06957236", "title": "Surgical Site Infection Outcomes in Natural Orifice Intracorporeal Anastomosis and Extraction (NICE) Procedure - The NICE Trial", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Diverticulitis", "Surgical Site Infection", "Surgical Site Infections", "Colorectal Surgery", "Robotic Surgical Procedures", "Clinical Trials", "Diverticulitis, Colonic", "Diverticulitis Colon", "Diverticulitis; Perforation, Bowel" ], "interventions": [], "intervention_types": [], "sponsor": "The Methodist Hospital Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 300, "start_date": "2025-04-02", "completion_date": "2026-12-30", "has_results": false, "last_update_posted_date": "2025-05-08", "last_synced_at": "2026-07-23T23:05:58.309Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06957236" }, { "nct_id": "NCT07467980", "title": "Endoscopic COlorectal Mucosal Evaluation of Oxygen Tension", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Anastomotic Leak Rectum", "Anastomotic Leak Large Intestine" ], "interventions": [ { "name": "A novel endoscopic imaging system that displays real-time oxygen saturation levels", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 80, "start_date": "2026-03-16", "completion_date": "2028-04", "has_results": false, "last_update_posted_date": "2026-06-11", "last_synced_at": "2026-07-23T23:05:58.309Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT07467980" }, { "nct_id": "NCT05725967", "title": "Endoscopic Metabolic and Bariatric Therapies", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Obesity", "Obesity, Morbid", "Obesity Associated Disorder", "Bariatric Surgery Candidate", "Fistula, Gastric", "Roux-en-y Anastomosis Site", "Ulcer, Gastric", "Abdominal Pain", "Abdominal Obesity", "Complication of Surgical Procedure", "Complication of Treatment", "Complication,Postoperative", "Weight Gain", "Weight Loss", "Leak, Anastomotic", "Delayed Gastric Emptying Following Procedure" ], "interventions": [ { "name": "Primary Obesity Endoscopic Procedures", "type": "PROCEDURE" }, { "name": "Endoscopic Revision of Bariatric Surgical Procedures", "type": "PROCEDURE" }, { "name": "Bariatric Surgery Procedures", "type": "PROCEDURE" }, { "name": "Endoscopic Sleeve Gastroplasty, Trans-oral Outlet Reduction", "type": "DEVICE" }, { "name": "Intragastric Balloon", "type": "DEVICE" }, { "name": "Primary obesity surgery endoluminal, Restorative obesity surgery endoluminal", "type": "DEVICE" }, { "name": "Argon Plasma Coagulation, Gastroplasty with Endoscopic Myotomy, Bariatric Endoscopic Antral Myotomy, Pylorus Sparing Antral Myotomy", "type": "DEVICE" }, { "name": "Aspiration Therapy", "type": "DEVICE" } ], "intervention_types": [ "PROCEDURE", "DEVICE" ], "sponsor": "Christopher C. Thompson, MD, MSc", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 5000, "start_date": "2022-07-08", "completion_date": "2029-05-28", "has_results": false, "last_update_posted_date": "2025-12-02", "last_synced_at": "2026-07-23T23:05:58.309Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05725967" } ] }