{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Bupivacaine&page=12", "query": { "intervention": "Bupivacaine", "page": 12 }, "page_size": 10 }, "pagination": { "page": 12, "page_size": 10, "total_count": 975, "total_pages": 98, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Bupivacaine&page=13&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Bupivacaine&page=11&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-31T08:53:29.014Z", "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": "NCT01126593", "title": "Post-Op Rotator Cuff Pain Study With Subacromial Bupivacaine Infusion", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Rotator Cuff Tear" ], "interventions": [ { "name": "0.5% bupivacaine", "type": "DRUG" }, { "name": "Normal Saline", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Orlando Health, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 96, "start_date": "2008-12", "completion_date": "2010-02", "has_results": true, "last_update_posted_date": "2014-11-07", "last_synced_at": "2026-10-31T08:53:29.014Z", "location_count": 1, "location_summary": "Orlando, Florida", "locations": [ { "city": "Orlando", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT01126593" }, { "nct_id": "NCT05285566", "title": "Pain Control for Undergoing Costal Cartilage Harvesting", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Nasal Surgery" ], "interventions": [ { "name": "Exparel", "type": "DRUG" }, { "name": "Xylocaine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2022-05-04", "completion_date": "2027-09", "has_results": false, "last_update_posted_date": "2026-09-11", "last_synced_at": "2026-10-31T08:53:29.014Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT05285566" }, { "nct_id": "NCT05216770", "title": "Understanding Disorder-specific Neural Pathophysiology in Laryngeal Dystonia and Voice Tremor", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Laryngeal Dystonia", "Spasmodic Dysphonia", "Tremor" ], "interventions": [ { "name": "Brain imaging", "type": "OTHER" }, { "name": "Laryngeal sensory block with topical bupivacaine", "type": "DRUG" } ], "intervention_types": [ "OTHER", "DRUG" ], "sponsor": "Massachusetts Eye and Ear Infirmary", "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": 165, "start_date": "2022-03-24", "completion_date": "2027-08-31", "has_results": false, "last_update_posted_date": "2025-12-02", "last_synced_at": "2026-10-31T08:53:29.014Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05216770" }, { "nct_id": "NCT07158736", "title": "Genicular Nerve Block for Knee Pain in the ED", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Knee Pain" ], "interventions": [ { "name": "Genicular nerve block with bupivacaine and corticosteroids", "type": "PROCEDURE" }, { "name": "Standard of Care", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "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": 8, "start_date": "2025-08-06", "completion_date": "2026-04-08", "has_results": false, "last_update_posted_date": "2026-10-02", "last_synced_at": "2026-10-31T08:53:29.014Z", "location_count": 4, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" }, { "city": "Philadelphia", "state": "Pennsylvania" }, { "city": "Philadelphia", "state": "Pennsylvania" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07158736" }, { "nct_id": "NCT04397458", "title": "Rescue Quadratus Lumborum Blocks for Post-cesarean Pain", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Morphine", "Analgesics", "Analgesics, Opioid", "Peripheral Nervous System Agents" ], "interventions": [ { "name": "Saline", "type": "DRUG" }, { "name": "Bupivacaine", "type": "DRUG" }, { "name": "Dexamethasone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "The University of Texas Health Science Center, Houston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "FEMALE", "summary": "18 Years to 50 Years · Female only" }, "enrollment_count": 0, "start_date": "2022-01-01", "completion_date": "2022-06-30", "has_results": false, "last_update_posted_date": "2023-11-03", "last_synced_at": "2026-10-31T08:53:29.014Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04397458" }, { "nct_id": "NCT04749615", "title": "Does PAI Reduce Pain After TKA Among Knee Arthroplasty Patients Receiving ACB & IPACK?", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Total Knee Athroplasty" ], "interventions": [ { "name": "Periarticular Injection (PAI)", "type": "DRUG" }, { "name": "Saline Control Periarticular Injection (PAI)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Hospital for Special Surgery, New York", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "25 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "25 Years to 80 Years" }, "enrollment_count": 94, "start_date": "2020-12-17", "completion_date": "2022-07-01", "has_results": true, "last_update_posted_date": "2024-12-27", "last_synced_at": "2026-10-31T08:53:29.014Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04749615" }, { "nct_id": "NCT03854344", "title": "Liposomal Bupivacaine Versus Lidocaine for Skin Graft Donor Site Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pain, Postoperative", "Burns" ], "interventions": [ { "name": "Lidocaine Hydrochloride", "type": "DRUG" }, { "name": "Liposomal bupivacaine", "type": "DRUG" }, { "name": "Bupivacaine Hydrochloride", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Kansas Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 74, "start_date": "2019-03-18", "completion_date": "2025-10-27", "has_results": true, "last_update_posted_date": "2026-03-31", "last_synced_at": "2026-10-31T08:53:29.014Z", "location_count": 1, "location_summary": "Kansas City, Kansas", "locations": [ { "city": "Kansas City", "state": "Kansas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03854344" }, { "nct_id": "NCT02356198", "title": "Exparel Transversus Abdominis Plane Block vs Intrathecal Analgesia In Colorectal Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Conditions Requiring Colorectal Surgery" ], "interventions": [ { "name": "EXPAREL", "type": "DRUG" }, { "name": "Intrathecal hydromorphone", "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": 209, "start_date": "2015-03", "completion_date": "2017-10", "has_results": true, "last_update_posted_date": "2019-03-07", "last_synced_at": "2026-10-31T08:53:29.014Z", "location_count": 1, "location_summary": "Jacksonville, Florida", "locations": [ { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02356198" }, { "nct_id": "NCT03066544", "title": "Status Migrainosus - Differentiating Between Responders and Non-responders", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Migraine" ], "interventions": [ { "name": "Bupivacaine", "type": "DRUG" }, { "name": "Naratriptan Pill", "type": "DRUG" }, { "name": "Dexamethasone", "type": "DRUG" }, { "name": "Ketorolac", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Hartford HealthCare", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 50, "start_date": "2016-11-30", "completion_date": "2020-06-30", "has_results": false, "last_update_posted_date": "2018-08-31", "last_synced_at": "2026-10-31T08:53:29.014Z", "location_count": 1, "location_summary": "Wethersfield, Connecticut", "locations": [ { "city": "Wethersfield", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT03066544" }, { "nct_id": "NCT03020563", "title": "Does Liposomal Bupivacaine Provide Improved Pain Management for ORIF of Midshaft Clavicle Fractures?", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Clavicle Fracture" ], "interventions": [ { "name": "Liposomal Bupivacaine", "type": "DRUG" }, { "name": "Bupivacaine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "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": 0, "start_date": "2017-08-23", "completion_date": "2018-01-01", "has_results": false, "last_update_posted_date": "2018-10-16", "last_synced_at": "2026-10-31T08:53:29.014Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT03020563" } ] }