{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=hydromorphone+hydrochloride", "query": { "intervention": "hydromorphone hydrochloride" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 182, "total_pages": 19, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=hydromorphone+hydrochloride&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-25T13:11:17.347Z", "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": "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": "2026-09-25T13:11:17.347Z", "location_count": 1, "location_summary": "Sacramento, California", "locations": [ { "city": "Sacramento", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04240626" }, { "nct_id": "NCT03427736", "title": "Anesthetics and Analgesics in Children", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Anesthesia", "Pain" ], "interventions": [ { "name": "Ketorolac Tromethamine", "type": "DRUG" }, { "name": "Hydromorphone", "type": "DRUG" }, { "name": "Ketamine", "type": "DRUG" }, { "name": "Oxycodone", "type": "DRUG" }, { "name": "Morphine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Chi Dang Hornik", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "0 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "0 Years to 17 Years" }, "enrollment_count": 551, "start_date": "2018-12-13", "completion_date": "2027-09-09", "has_results": false, "last_update_posted_date": "2026-08-05", "last_synced_at": "2026-09-25T13:11:17.347Z", "location_count": 11, "location_summary": "Stanford, California • Aurora, Colorado • Wilmington, Delaware + 7 more", "locations": [ { "city": "Stanford", "state": "California" }, { "city": "Aurora", "state": "Colorado" }, { "city": "Wilmington", "state": "Delaware" }, { "city": "Chicago", "state": "Illinois" }, { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT03427736" }, { "nct_id": "NCT06406400", "title": "Drug-Drug Interaction and Safety of AZD4041 Study (Part 1) and Efficacy, Safety, Pharmacokinetics and Pharmacodynamics of AZD4041 Study in Opioid Use Disorder (Part 2).", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Opioid Use Disorder" ], "interventions": [ { "name": "AZD4041", "type": "DRUG" }, { "name": "Itraconazole", "type": "DRUG" }, { "name": "Buprenorphine", "type": "DRUG" }, { "name": "Buprenorphine / Naloxone", "type": "DRUG" }, { "name": "Hydromorphone", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "AstraZeneca", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 15, "start_date": "2024-05-13", "completion_date": "2024-07-31", "has_results": false, "last_update_posted_date": "2025-03-26", "last_synced_at": "2026-09-25T13:11:17.347Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT06406400" }, { "nct_id": "NCT00413582", "title": "Pain Management for Pectus Excavatum Repair", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postoperative Pain" ], "interventions": [ { "name": "Epidural Analgesia", "type": "DRUG" }, { "name": "Patient-Controlled IV Analgesia", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Children's Mercy Hospital Kansas City", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "8 Years to 18 Years" }, "enrollment_count": 110, "start_date": "2006-10", "completion_date": "2010-10", "has_results": true, "last_update_posted_date": "2012-01-16", "last_synced_at": "2026-09-25T13:11:17.347Z", "location_count": 1, "location_summary": "Kansas City, Missouri", "locations": [ { "city": "Kansas City", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT00413582" }, { "nct_id": "NCT02107339", "title": "Methadone and Hydromorphone For Spinal Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Hydromorphone Use", "Acute Postoperative Pain", "Patient Satisfaction", "Chronic Persistent Surgical Pain" ], "interventions": [ { "name": "Methadone", "type": "DRUG" }, { "name": "Hydromorphone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Endeavor Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 120, "start_date": "2014-03", "completion_date": "2017-09", "has_results": true, "last_update_posted_date": "2019-09-30", "last_synced_at": "2026-09-25T13:11:17.347Z", "location_count": 1, "location_summary": "Evanston, Illinois", "locations": [ { "city": "Evanston", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT02107339" }, { "nct_id": "NCT01598545", "title": "Hydromorphone and C-section", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Postoperative Pain" ], "interventions": [ { "name": "Hydromorphone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "FEMALE", "summary": "18 Years to 40 Years · Female only" }, "enrollment_count": 20, "start_date": "2013-02", "completion_date": "2014-09", "has_results": true, "last_update_posted_date": "2014-12-17", "last_synced_at": "2026-09-25T13:11:17.347Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01598545" }, { "nct_id": "NCT06411795", "title": "Rectus Sheath Block With Liposomal Bupivacaine Versus Thoracic Epidural Analgesia for Pain Control Following Pancreatoduodenectomy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Duodenal Neoplasm", "Pancreatic Neoplasm" ], "interventions": [ { "name": "Bupivacaine", "type": "DRUG" }, { "name": "Hydromorphone", "type": "DRUG" }, { "name": "Iopamidol", "type": "DRUG" }, { "name": "Liposomal Bupivacaine", "type": "DRUG" }, { "name": "Medical Chart Review", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Thoracic Epidural Analgesia", "type": "DRUG" }, { "name": "Ultrasound Imaging", "type": "PROCEDURE" }, { "name": "X-Ray Imaging", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "OTHER", "PROCEDURE" ], "sponsor": "Masonic Cancer Center, University of Minnesota", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 78, "start_date": "2023-11-10", "completion_date": "2028-01-01", "has_results": false, "last_update_posted_date": "2026-02-03", "last_synced_at": "2026-09-25T13:11:17.347Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT06411795" }, { "nct_id": "NCT01932554", "title": "Abciximab (ReoPro) as a Therapeutic Intervention for Sickle Cell Vaso-Occlusive Pain Crisis", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Sickle Cell Disease", "Hb-SS Disease With Vasoocclusive Pain", "Hemoglobin SS Disease With Vasoocclusive Crisis", "Other Sickle Cell Disease With Vaso-Occlusive Pain", "Hemoglobin SS Disease With Crisis" ], "interventions": [ { "name": "Abciximab", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Intravenous hydration", "type": "OTHER" }, { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Parenteral narcotic", "type": "DRUG" }, { "name": "Incentive spirometry", "type": "OTHER" }, { "name": "Supplemental oxygen", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "St. Louis University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "5 Years", "maximum_age": "25 Years", "sex": "ALL", "summary": "5 Years to 25 Years" }, "enrollment_count": 0, "start_date": "2013-11", "completion_date": "2015-03", "has_results": false, "last_update_posted_date": "2015-03-26", "last_synced_at": "2026-09-25T13:11:17.347Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT01932554" }, { "nct_id": "NCT05027919", "title": "Assessing a Clinically-meaningful Opioid Withdrawal Phenotype", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Opioid Withdrawal", "Opioid Use Disorder", "Opioid Craving" ], "interventions": [ { "name": "Hydromorphone", "type": "DRUG" }, { "name": "Naloxone + lofexidine pretreatment", "type": "DRUG" }, { "name": "Naloxone + placebo pretreatment", "type": "DRUG" }, { "name": "Lofexidine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Maryland, Baltimore", "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": 60, "start_date": "2021-12-01", "completion_date": "2027-02-28", "has_results": false, "last_update_posted_date": "2025-09-12", "last_synced_at": "2026-09-25T13:11:17.347Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT05027919" }, { "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": "2026-09-25T13:11:17.347Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05279898" } ] }