{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Oxycodone+%28rescue+medication%29", "query": { "intervention": "Oxycodone (rescue medication)" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 19, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Oxycodone+%28rescue+medication%29&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-26T05:06:18.037Z", "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": "NCT02028715", "title": "Efficacy of IV Acetaminophen for Pain Management", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Post-operative Pain" ], "interventions": [ { "name": "Placebo", "type": "DRUG" }, { "name": "IV acetaminophen", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Aultman Health Foundation", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "FEMALE", "summary": "18 Years to 85 Years · Female only" }, "enrollment_count": 68, "start_date": "2013-12-24", "completion_date": "2014-06-04", "has_results": true, "last_update_posted_date": "2019-01-16", "last_synced_at": "2026-09-26T05:06:18.037Z", "location_count": 1, "location_summary": "Canton, Ohio", "locations": [ { "city": "Canton", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02028715" }, { "nct_id": "NCT04240626", "title": "Multimodal Analgesia Effect on Post Surgical Patient", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Obesity, Morbid", "Surgery", "Bariatric Surgery Candidate" ], "interventions": [ { "name": "Neurontin", "type": "DRUG" }, { "name": "Dilaudid Injectable Product", "type": "DRUG" }, { "name": "Marcaine Injectable Product", "type": "DRUG" }, { "name": "Oxycodone Hydrochloride", "type": "DRUG" }, { "name": "Hycet 7.5Mg-325Mg/15Ml Solution", "type": "DRUG" }, { "name": "Zofran Injection", "type": "DRUG" }, { "name": "Scopolamine patch", "type": "DRUG" }, { "name": "Ativan", "type": "DRUG" }, { "name": "Flexeril Oral Product", "type": "DRUG" }, { "name": "Tylenol Suspension", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of California, Davis", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "35 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "35 Years to 65 Years · Female only" }, "enrollment_count": 60, "start_date": "2021-01-20", "completion_date": "2025-06-24", "has_results": false, "last_update_posted_date": "2026-09-14", "last_synced_at": "2026-09-26T05:06:18.037Z", "location_count": 1, "location_summary": "Sacramento, California", "locations": [ { "city": "Sacramento", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04240626" }, { "nct_id": "NCT05279898", "title": "Perioperative Multimodal General AnesTHesia Focusing on Specific CNS Targets in Patients Undergoing carDiac surgERies", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postoperative Delirium", "Hemodynamic Instability", "Pain", "Neurocognitive Dysfunction" ], "interventions": [ { "name": "EEG Monitoring", "type": "DEVICE" }, { "name": "Ropivacaine", "type": "DRUG" }, { "name": "Ketamine", "type": "DRUG" }, { "name": "Remifentanil", "type": "DRUG" }, { "name": "Dexmedetomidine", "type": "DRUG" }, { "name": "Rocuronium", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "DRUG" ], "sponsor": "Beth Israel Deaconess Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": null, "sex": "ALL", "summary": "60 Years and older" }, "enrollment_count": 70, "start_date": "2023-02-28", "completion_date": "2024-12-31", "has_results": true, "last_update_posted_date": "2025-11-26", "last_synced_at": "2026-09-26T05:06:18.037Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05279898" }, { "nct_id": "NCT07796152", "title": "Suzetrigine vs. Standard Care Pain Relief Following Outpatient Knee Replacement Surgery", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Knee Arthroplasty, Total", "Post Operative Pain, Acute", "Opioid Consumption, Postoperative" ], "interventions": [ { "name": "Suzetrigine", "type": "DRUG" }, { "name": "Opioid standard care pain medicine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Endeavor Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2026-09", "completion_date": "2028-01", "has_results": false, "last_update_posted_date": "2026-09-02", "last_synced_at": "2026-09-26T05:06:18.037Z", "location_count": 1, "location_summary": "Skokie, Illinois", "locations": [ { "city": "Skokie", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT07796152" }, { "nct_id": "NCT06973785", "title": "Non-Narcotic Pain Control After ACL Reconstruction", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "ACL - Anterior Cruciate Ligament Rupture", "ACL Injuries" ], "interventions": [ { "name": "dispense of study drug", "type": "DRUG" }, { "name": "Ketorolac", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "15 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "15 Years to 55 Years" }, "enrollment_count": 30, "start_date": "2025-07-15", "completion_date": "2027-06-15", "has_results": false, "last_update_posted_date": "2026-08-24", "last_synced_at": "2026-09-26T05:06:18.037Z", "location_count": 3, "location_summary": "Coral Springs, Florida • Garfield, Ohio • Strongsville, Ohio", "locations": [ { "city": "Coral Springs", "state": "Florida" }, { "city": "Garfield", "state": "Ohio" }, { "city": "Strongsville", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT06973785" }, { "nct_id": "NCT05200806", "title": "A Prospective Pilot Study of a Non-Narcotic Post-Operative Course After Colectomy", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Analgesia", "Post-Operative Pain", "Breakthrough Pain", "Colectomy" ], "interventions": [ { "name": "Non-Narcotic ERAS Post-Operative Pain Management", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Vermont", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 25, "start_date": "2022-02-07", "completion_date": "2024-10", "has_results": false, "last_update_posted_date": "2022-10-14", "last_synced_at": "2026-09-26T05:06:18.037Z", "location_count": 1, "location_summary": "Burlington, Vermont", "locations": [ { "city": "Burlington", "state": "Vermont" } ], "official_url": "https://clinicaltrials.gov/study/NCT05200806" }, { "nct_id": "NCT07348627", "title": "Opioid-Sparing Joint Replacement", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Pain Management", "Opioid Consumption" ], "interventions": [ { "name": "Placebo", "type": "DRUG" }, { "name": "Oxycodone 5 mg", "type": "DRUG" }, { "name": "Multimodal Non-Opioid Analgesia", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2026-03-19", "completion_date": "2028-08", "has_results": false, "last_update_posted_date": "2026-04-17", "last_synced_at": "2026-09-26T05:06:18.037Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07348627" }, { "nct_id": "NCT07219888", "title": "Comparison of Suzetrigine and Oxycodone for Postoperative Pain After Primary Total Knee Arthroplasty", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Osteoarthritis (OA) of the Knee" ], "interventions": [ { "name": "oral suzetrigine", "type": "DRUG" }, { "name": "oral Oxycodone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Louisville", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "21 Years to 89 Years" }, "enrollment_count": 140, "start_date": "2026-02-09", "completion_date": "2027-04-30", "has_results": false, "last_update_posted_date": "2026-05-04", "last_synced_at": "2026-09-26T05:06:18.037Z", "location_count": 1, "location_summary": "Louisville, Kentucky", "locations": [ { "city": "Louisville", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT07219888" }, { "nct_id": "NCT02625181", "title": "Real-time Decision Support for Postoperative Nausea and Vomiting (PONV) Prophylaxis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postoperative Nausea and Vomiting" ], "interventions": [ { "name": "Automated recommendation at the start of the case", "type": "PROCEDURE" }, { "name": "Automated notification at the start of surgery", "type": "PROCEDURE" }, { "name": "Preoperative recommendations: by email", "type": "PROCEDURE" }, { "name": "Automated notification at the end of surgery", "type": "PROCEDURE" }, { "name": "Anesthesia Information Management System (AIMS)", "type": "DEVICE" }, { "name": "Perioperative Data Warehouse (PDW)", "type": "DEVICE" }, { "name": "General anesthesia", "type": "PROCEDURE" }, { "name": "Elective surgery", "type": "PROCEDURE" }, { "name": "Propofol", "type": "DRUG" }, { "name": "Sevoflurane", "type": "DRUG" }, { "name": "Isoflurane", "type": "DRUG" }, { "name": "Desflurane", "type": "DRUG" }, { "name": "Scopolamine", "type": "DRUG" }, { "name": "Droperidol", "type": "DRUG" }, { "name": "Haloperidol", "type": "DRUG" }, { "name": "Dexamethasone", "type": "DRUG" }, { "name": "Promethazine", "type": "DRUG" }, { "name": "Meclizine", "type": "DRUG" }, { "name": "Aprepitant", "type": "DRUG" }, { "name": "Metoclopramide", "type": "DRUG" }, { "name": "Fentanyl", "type": "DRUG" }, { "name": "Sufentanil", "type": "DRUG" }, { "name": "Alfentanil", "type": "DRUG" }, { "name": "Remifentanil", "type": "DRUG" }, { "name": "Morphine", "type": "DRUG" }, { "name": "Meperidine", "type": "DRUG" }, { "name": "Hydromorphone", "type": "DRUG" }, { "name": "Methadone", "type": "DRUG" }, { "name": "Oxycodone", "type": "DRUG" }, { "name": "Oxymorphone", "type": "DRUG" }, { "name": "Hydrocodone", "type": "DRUG" }, { "name": "Ketamine", "type": "DRUG" }, { "name": "Ondansetron", "type": "DRUG" }, { "name": "Granisetron", "type": "DRUG" }, { "name": "Dolasetron mesylate", "type": "DRUG" }, { "name": "Palonosetron", "type": "DRUG" }, { "name": "Tropisetron", "type": "DRUG" }, { "name": "Ramosetron", "type": "DRUG" } ], "intervention_types": [ "PROCEDURE", "DEVICE", "DRUG" ], "sponsor": "Vanderbilt University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 27034, "start_date": "2016-07", "completion_date": "2017-11-30", "has_results": true, "last_update_posted_date": "2019-03-07", "last_synced_at": "2026-09-26T05:06:18.037Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02625181" }, { "nct_id": "NCT05813847", "title": "Herniorrhaphy for Postoperative Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Hernia, Inguinal", "Post Operative Pain" ], "interventions": [ { "name": "local anaesthetic injection of CPL-01", "type": "DRUG" }, { "name": "Morphine (rescue medication)", "type": "DRUG" }, { "name": "Acetaminophen (rescue medication)", "type": "DRUG" }, { "name": "Oxycodone (rescue medication)", "type": "DRUG" }, { "name": "local anaesthetic injection of placebo", "type": "DRUG" }, { "name": "local anaesthetic injection of ropivacaine HCl", "type": "DRUG" }, { "name": "Open inguinal hernia repair", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "PROCEDURE" ], "sponsor": "Cali Pharmaceuticals LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 518, "start_date": "2023-04-18", "completion_date": "2025-10-06", "has_results": false, "last_update_posted_date": "2026-04-30", "last_synced_at": "2026-09-26T05:06:18.037Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT05813847" } ] }