{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Post+Surgery+Patients&page=28", "query": { "condition": "Post Surgery Patients", "page": 28 }, "page_size": 10 }, "pagination": { "page": 28, "page_size": 10, "total_count": 958, "total_pages": 96, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Post+Surgery+Patients&page=29&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Post+Surgery+Patients&page=27&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-14T14:28:32.400Z", "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": "NCT02047474", "title": "Combination Chemotherapy Before and After Surgery in Treating Patients With Localized Pancreatic Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Acinar Cell Adenocarcinoma of the Pancreas", "Duct Cell Adenocarcinoma of the Pancreas", "Stage I Pancreatic Cancer", "Stage IIA Pancreatic Cancer", "Stage IIB Pancreatic Cancer" ], "interventions": [ { "name": "oxaliplatin", "type": "DRUG" }, { "name": "leucovorin calcium", "type": "DRUG" }, { "name": "irinotecan hydrochloride", "type": "DRUG" }, { "name": "fluorouracil", "type": "DRUG" }, { "name": "therapeutic conventional surgery", "type": "PROCEDURE" }, { "name": "laboratory biomarker analysis", "type": "OTHER" } ], "intervention_types": [ "DRUG", "PROCEDURE", "OTHER" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 46, "start_date": "2014-03-25", "completion_date": "2024-01-14", "has_results": true, "last_update_posted_date": "2026-03-06", "last_synced_at": "2026-10-14T14:28:32.400Z", "location_count": 9, "location_summary": "Fairfield, Connecticut • Guilford, Connecticut • Hartford, Connecticut + 6 more", "locations": [ { "city": "Fairfield", "state": "Connecticut" }, { "city": "Guilford", "state": "Connecticut" }, { "city": "Hartford", "state": "Connecticut" }, { "city": "New Haven", "state": "Connecticut" }, { "city": "North Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT02047474" }, { "nct_id": "NCT07391735", "title": "Post-Surgery Wound Healing Tracking With MyHealthPal App", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Wound Infection and Wound Healing" ], "interventions": [ { "name": "MyHealthPal App", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Brigham and Women's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 150, "start_date": "2026-03-27", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2026-08-12", "last_synced_at": "2026-10-14T14:28:32.400Z", "location_count": 1, "location_summary": "Chestnut Hill, Massachusetts", "locations": [ { "city": "Chestnut Hill", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07391735" }, { "nct_id": "NCT03529019", "title": "Nutrition in Patient With Critical Limb Ischemia", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Critical Limb Ischemia", "Malnutrition", "Nutritional Supplements" ], "interventions": [ { "name": "Ensure Surgery Immunonutrition Shake", "type": "DRUG" }, { "name": "Ensure Enlive Advanced Nutrition Shake", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Boston Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 30, "start_date": "2018-10-02", "completion_date": "2027-08", "has_results": false, "last_update_posted_date": "2026-09-29", "last_synced_at": "2026-10-14T14:28:32.400Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03529019" }, { "nct_id": "NCT01082575", "title": "Oxygen Monitoring of Patients After Surgery on the Hospital General Care Floor", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Sleep Disordered Breathing" ], "interventions": [ { "name": "Oxygen Monitoring", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Medtronic - MITG", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2010-02", "completion_date": "2010-08", "has_results": true, "last_update_posted_date": "2014-08-07", "last_synced_at": "2026-10-14T14:28:32.400Z", "location_count": 3, "location_summary": "Santa Barbara, California • New Orleans, Louisiana • Fort Worth, Texas", "locations": [ { "city": "Santa Barbara", "state": "California" }, { "city": "New Orleans", "state": "Louisiana" }, { "city": "Fort Worth", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01082575" }, { "nct_id": "NCT05358522", "title": "Increasing Implementation of Post-Operative Opioid Prescribing Guidelines", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Surgery", "Opioid Use", "Opioid Misuse", "Prescription Opioid Misuse" ], "interventions": [ { "name": "Opioid Prescribing Report Cards", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 26562, "start_date": "2022-06-01", "completion_date": "2023-11-05", "has_results": false, "last_update_posted_date": "2024-02-28", "last_synced_at": "2026-10-14T14:28:32.400Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05358522" }, { "nct_id": "NCT01689922", "title": "The Effectiveness of Anti-Gravity Treadmill Training", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Lumbar Degenerative Disc Disease" ], "interventions": [ { "name": "AlterG", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Justin Parker Neurological Institute", "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": 27, "start_date": "2012-06", "completion_date": "2016-08", "has_results": false, "last_update_posted_date": "2017-03-01", "last_synced_at": "2026-10-14T14:28:32.400Z", "location_count": 1, "location_summary": "Boulder, Colorado", "locations": [ { "city": "Boulder", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT01689922" }, { "nct_id": "NCT03532256", "title": "Post-op Crowd Sourcing Health Data Via Text-messaging", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Orthopedic Surgery", "Opioid Use", "Acute Injuries Knee", "Neurosurgery", "Surgery" ], "interventions": [ { "name": "Observation", "type": "BEHAVIORAL" }, { "name": "Text to online survey", "type": "BEHAVIORAL" }, { "name": "Bi-directional text script", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 127, "start_date": "2019-07-01", "completion_date": "2019-09-16", "has_results": true, "last_update_posted_date": "2025-06-04", "last_synced_at": "2026-10-14T14:28:32.400Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03532256" }, { "nct_id": "NCT00473356", "title": "Nutritional Effect of an Amino Acid Mixture on Lean Body Mass (LBM) in Post-bariatric Surgery Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity", "Post-gastric Bypass" ], "interventions": [ { "name": "receive amino acid supplement", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 30, "start_date": "2007-06", "completion_date": "2010-01", "has_results": false, "last_update_posted_date": "2013-11-19", "last_synced_at": "2026-10-14T14:28:32.400Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT00473356" }, { "nct_id": "NCT06538584", "title": "Dex +/- Caffeine Sedation in a Post-MRI Recovery in a Pediatric Population", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Enhanced Recovery After Surgery in a Pediatric Population" ], "interventions": [ { "name": "Caffeine citrate 15mg/kg", "type": "DRUG" }, { "name": "0.9% Sodium Citrate", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "3 Years", "maximum_age": "12 Years", "sex": "ALL", "summary": "3 Years to 12 Years" }, "enrollment_count": 100, "start_date": "2024-09-09", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2025-09-12", "last_synced_at": "2026-10-14T14:28:32.400Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06538584" }, { "nct_id": "NCT06350916", "title": "Application to Improve Patient Engagement and Decrease Postoperative Opioid Consumption in Patients for Colorectal Surgery", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Colorectal Surgery" ], "interventions": [ { "name": "SeamlessMD® Mobile Application", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 75, "start_date": "2021-01-28", "completion_date": "2021-10-01", "has_results": false, "last_update_posted_date": "2024-05-08", "last_synced_at": "2026-10-14T14:28:32.400Z", "location_count": 1, "location_summary": "Charlotte, North Carolina", "locations": [ { "city": "Charlotte", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06350916" } ] }