{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Post+Operative+Nutrition&page=2", "query": { "condition": "Post Operative Nutrition", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Post+Operative+Nutrition&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-07-23T01:02:16.741Z", "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": "NCT03520803", "title": "Enhanced Recovery After Surgery in Laparoscopic Sleeve Gastrectomy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity" ], "interventions": [ { "name": "Enhanced recovery after surgery protocol", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Hartford Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 132, "start_date": "2019-01-26", "completion_date": "2020-01-30", "has_results": false, "last_update_posted_date": "2021-02-09", "last_synced_at": "2026-07-23T01:02:16.741Z", "location_count": 1, "location_summary": "Hartford, Connecticut", "locations": [ { "city": "Hartford", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT03520803" }, { "nct_id": "NCT02682381", "title": "Short Bowel Syndrome Research Study for Children Up To 17 Years of Age on Parenteral Nutrition", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Short Bowel Syndrome" ], "interventions": [ { "name": "Teduglutide 0.05mg/kg", "type": "DRUG" }, { "name": "Teduglutide 0.025 mg/kg", "type": "DRUG" }, { "name": "Standard of Care", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Shire", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "0 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "0 Years to 17 Years" }, "enrollment_count": 59, "start_date": "2016-06-23", "completion_date": "2017-08-18", "has_results": true, "last_update_posted_date": "2021-06-09", "last_synced_at": "2026-07-23T01:02:16.741Z", "location_count": 18, "location_summary": "Los Angeles, California • San Francisco, California • Washington D.C., District of Columbia + 14 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT02682381" }, { "nct_id": "NCT01460667", "title": "Efficacy of IV Acetaminophen in Acute Post-Operative Pain Control in Laparoscopic Roux-en-Y Gastric Bypass Surgery (LRYGBP) Patients", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Morbid Obesity" ], "interventions": [ { "name": "IV acetaminophen", "type": "DRUG" }, { "name": "IV normal saline", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "McLaren Regional Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 85, "start_date": "2011-10", "completion_date": null, "has_results": false, "last_update_posted_date": "2011-10-27", "last_synced_at": "2026-07-23T01:02:16.741Z", "location_count": 1, "location_summary": "Flint, Michigan", "locations": [ { "city": "Flint", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT01460667" }, { "nct_id": "NCT03054948", "title": "SMOFLipid in Patients Who Are Intralipid Intolerant", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Home Parenteral Nutrition", "Short Bowel Syndrome" ], "interventions": [ { "name": "SMOFLipid", "type": "DRUG" }, { "name": "Standard therapy", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2017-02-01", "completion_date": "2018-03-20", "has_results": false, "last_update_posted_date": "2018-03-22", "last_synced_at": "2026-07-23T01:02:16.741Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT03054948" }, { "nct_id": "NCT01576003", "title": "Enteral Glutamine in Reducing Bloodstream Infections in Short Bowel Syndrome Infants", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bloodstream Infections", "Short Bowel Syndrome", "Development", "Nutrition", "Biological Markers" ], "interventions": [ { "name": "Glutamine", "type": "DRUG" }, { "name": "L-alanine", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DRUG", "DIETARY_SUPPLEMENT" ], "sponsor": "Children's Hospital Medical Center, Cincinnati", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "6 Weeks", "maximum_age": "12 Months", "sex": "ALL", "summary": "6 Weeks to 12 Months" }, "enrollment_count": 10, "start_date": "2012-04", "completion_date": "2015-06", "has_results": true, "last_update_posted_date": "2020-06-11", "last_synced_at": "2026-07-23T01:02:16.741Z", "location_count": 2, "location_summary": "Ann Arbor, Michigan • Cincinnati, Ohio", "locations": [ { "city": "Ann Arbor", "state": "Michigan" }, { "city": "Cincinnati", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01576003" }, { "nct_id": "NCT01858051", "title": "Vitamin D Status in Lower Extremity Joint Replacement Surgery Patients", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypovitaminosis D" ], "interventions": [ { "name": "Cholecalciferol", "type": "DIETARY_SUPPLEMENT" }, { "name": "Placebo", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 0, "start_date": "2015-01", "completion_date": "2017-06", "has_results": false, "last_update_posted_date": "2017-03-30", "last_synced_at": "2026-07-23T01:02:16.741Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01858051" }, { "nct_id": "NCT04743960", "title": "Assessing Metabolic and Sleep Consequences of Overnight Home Parenteral Nutrition", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Feeding Patterns", "Sleep", "Glucose Intolerance", "Short Bowel Syndrome" ], "interventions": [ { "name": "Time-of-day of parenteral nutrition provision", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "79 Years", "sex": "ALL", "summary": "18 Years to 79 Years" }, "enrollment_count": 20, "start_date": "2021-10-05", "completion_date": "2022-10-24", "has_results": false, "last_update_posted_date": "2025-09-25", "last_synced_at": "2026-07-23T01:02:16.741Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04743960" }, { "nct_id": "NCT01083108", "title": "Effects of Caloric Restriction Alone Versus Postoperative Caloric Restriction Following Bariatric Surgery on Glucose Metabolism in Patients With Diabetes Mellitus", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Obesity", "Bariatric Surgery", "Morbid Obesity", "Diabetes Mellitus Type 2", "Diet Therapy" ], "interventions": [ { "name": "Roux-en-Y Gastric Bypass", "type": "OTHER" }, { "name": "Caloric Restriction", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 5, "start_date": "2011-03-31", "completion_date": "2019-12-13", "has_results": false, "last_update_posted_date": "2019-12-17", "last_synced_at": "2026-07-23T01:02:16.741Z", "location_count": 3, "location_summary": "Baltimore, Maryland • Bethesda, Maryland • Nashville, Tennessee", "locations": [ { "city": "Baltimore", "state": "Maryland" }, { "city": "Bethesda", "state": "Maryland" }, { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT01083108" }, { "nct_id": "NCT02987569", "title": "Teen and Young Adult Connections for Support From Multidisciplinary Professionals & Peers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Short Bowel Syndrome", "Malabsorption", "Malnutrition" ], "interventions": [ { "name": "mConnect plus mobile connections to multidisciplinary professionals & peers", "type": "BEHAVIORAL" }, { "name": "iPad use plus one mobile connections to multidisciplinary professionals & peers", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Kansas Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "13 Years", "maximum_age": "30 Years", "sex": "ALL", "summary": "13 Years to 30 Years" }, "enrollment_count": 83, "start_date": "2016-07", "completion_date": "2020-06", "has_results": false, "last_update_posted_date": "2020-12-02", "last_synced_at": "2026-07-23T01:02:16.741Z", "location_count": 1, "location_summary": "Kansas City, Kansas", "locations": [ { "city": "Kansas City", "state": "Kansas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02987569" }, { "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": "2026-07-23T01:02:16.741Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05725967" } ] }