{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Operative+Time&page=2", "query": { "condition": "Operative Time", "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=Operative+Time&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-07-23T00:22:44.608Z", "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": "NCT05002829", "title": "Restricted or Liberal Antibiotics After Appendectomy - Denver Health", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Appendicitis" ], "interventions": [ { "name": "Restricted Duration of SOC Antibiotic Use", "type": "OTHER" }, { "name": "Liberal Duration of SOC Antibiotic Use", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Denver Health and Hospital Authority", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 657, "start_date": "2021-11-01", "completion_date": "2025-07-16", "has_results": false, "last_update_posted_date": "2026-06-30", "last_synced_at": "2026-07-23T00:22:44.608Z", "location_count": 1, "location_summary": "Denver, Colorado", "locations": [ { "city": "Denver", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT05002829" }, { "nct_id": "NCT02623660", "title": "Microcurrent Stimulation Reduces Post-Operative Swelling and Healing Time Following Knee Replacement Surgery", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Osteoarthritis of Knee", "Edema", "Wounds and Injuries" ], "interventions": [ { "name": "ODIN1", "type": "DEVICE" }, { "name": "Standard Care", "type": "OTHER" }, { "name": "Diagnostic Device Testing", "type": "DEVICE" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Bioelectric Research Corporation", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 40, "start_date": "2016-01", "completion_date": "2016-10", "has_results": false, "last_update_posted_date": "2016-01-12", "last_synced_at": "2026-07-23T00:22:44.608Z", "location_count": 2, "location_summary": "Las Vegas, Nevada", "locations": [ { "city": "Las Vegas", "state": "Nevada" }, { "city": "Las Vegas", "state": "Nevada" } ], "official_url": "https://clinicaltrials.gov/study/NCT02623660" }, { "nct_id": "NCT05532150", "title": "Conservative Versus Operative - First Time Shoulder Dislocations", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Shoulder Dislocation" ], "interventions": [ { "name": "Arthroscopic Bankart repair", "type": "PROCEDURE" }, { "name": "Physical therapy", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Years", "maximum_age": null, "sex": "ALL", "summary": "12 Years and older" }, "enrollment_count": 200, "start_date": "2026-09", "completion_date": "2032-09", "has_results": false, "last_update_posted_date": "2025-09-22", "last_synced_at": "2026-07-23T00:22:44.608Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05532150" }, { "nct_id": "NCT02741531", "title": "The Effect of Partial Bladder Filling on Post-operative Time to Void in Minimally Invasive Gynecologic Procedures", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hysterectomy", "Myomectomy" ], "interventions": [ { "name": "Bladder filled with saline solution", "type": "OTHER" }, { "name": "saline solution", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "George Washington University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "18 Years to 65 Years · Female only" }, "enrollment_count": 100, "start_date": "2016-03", "completion_date": "2017-07-27", "has_results": false, "last_update_posted_date": "2023-05-19", "last_synced_at": "2026-07-23T00:22:44.608Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02741531" }, { "nct_id": "NCT03471377", "title": "Improving Planned Surgical Case Duration Accuracy by Leveraging the EHR and Predictive Modeling", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Operative Time" ], "interventions": [ { "name": "standard scheduling process", "type": "OTHER" }, { "name": "assigned a planned case duration value from predictive model", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 683, "start_date": "2018-03-05", "completion_date": "2022-03-15", "has_results": false, "last_update_posted_date": "2022-03-17", "last_synced_at": "2026-07-23T00:22:44.608Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03471377" }, { "nct_id": "NCT01023724", "title": "A Comparison of Post Phacoemulsification Aqueous Flare in Patients Using Ketorolac 0.45% 2 Times Daily (BID) and Bromfenac 0.09% 2 Times Daily (BID)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Post Operative Anterior Chamber Inflammation (Flare)" ], "interventions": [ { "name": "Ketorolac Tromethamine 0.45%", "type": "DRUG" }, { "name": "Bromfenac 0.09%", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Bucci Laser Vision Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 50, "start_date": "2009-12", "completion_date": "2010-02", "has_results": true, "last_update_posted_date": "2011-08-26", "last_synced_at": "2026-07-23T00:22:44.608Z", "location_count": 1, "location_summary": "Wilkes-Barre, Pennsylvania", "locations": [ { "city": "Wilkes-Barre", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01023724" }, { "nct_id": "NCT00443040", "title": "Asimadoline for the Treatment of Post-Operative Ileus", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Post-Operative Ileus" ], "interventions": [ { "name": "Asimadoline", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Tioga Pharmaceuticals", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 35, "start_date": "2007-01", "completion_date": "2008-02", "has_results": true, "last_update_posted_date": "2012-01-06", "last_synced_at": "2026-07-23T00:22:44.608Z", "location_count": 4, "location_summary": "Burlington, Massachusetts • St Louis, Missouri • Cleveland, Ohio + 1 more", "locations": [ { "city": "Burlington", "state": "Massachusetts" }, { "city": "St Louis", "state": "Missouri" }, { "city": "Cleveland", "state": "Ohio" }, { "city": "Wynnewood", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00443040" }, { "nct_id": "NCT02730728", "title": "Single Shot vs 24hr vs 48hr Continuous Adductor Canal Block After TKA", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Total Knee Arthroplasty", "Osteoarthritis", "Post Operative Pain Control" ], "interventions": [ { "name": "20ml bolus of 0.5% ropivicaine", "type": "DRUG" }, { "name": "0.2% Ropivicaine at 8 milliliter/hour", "type": "DRUG" }, { "name": "5ml bolus of 0.5% ropivicaine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "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": 159, "start_date": "2015-11-01", "completion_date": "2017-01-01", "has_results": true, "last_update_posted_date": "2018-10-31", "last_synced_at": "2026-07-23T00:22:44.608Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02730728" }, { "nct_id": "NCT04597372", "title": "Impact of Tamsulosin on Post-Operative Urinary Retention Following Pelvic Reconstructive Surgery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Urinary Retention Postoperative" ], "interventions": [ { "name": "Tamsulosin", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 154, "start_date": "2021-11-03", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-03-20", "last_synced_at": "2026-07-23T00:22:44.608Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04597372" }, { "nct_id": "NCT00739583", "title": "Visibility of Site Marking for Surgical Time Out With Two Different Skin Preparation Solutions", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Arthroplasty, Replacement, Hip" ], "interventions": [ { "name": "CHG 2% w/v and IPA 70% v/v", "type": "DRUG" }, { "name": "Iodophor 0.7% and IPA 74% w/w", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 20, "start_date": "2008-08", "completion_date": "2009-08", "has_results": true, "last_update_posted_date": "2013-07-10", "last_synced_at": "2026-07-23T00:22:44.608Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT00739583" } ] }