{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=ketorolac+and+lidocaine", "query": { "intervention": "ketorolac and lidocaine" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 22, "total_pages": 3, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=ketorolac+and+lidocaine&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-10-05T13:23:03.950Z", "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": "NCT03540030", "title": "Opioid-Free Shoulder Arthroplasty", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Opioid Use", "Shoulder Osteoarthritis", "Avascular Necrosis", "Rotator Cuff Tear", "Arthritis;Inflammatory" ], "interventions": [ { "name": "Gabapentin", "type": "DRUG" }, { "name": "Celecoxib", "type": "DRUG" }, { "name": "toradol", "type": "DRUG" }, { "name": "acetaminophen", "type": "DRUG" }, { "name": "regional block", "type": "DRUG" }, { "name": "propofol", "type": "DRUG" }, { "name": "IV lidocaine", "type": "DRUG" }, { "name": "rocuronium", "type": "DRUG" }, { "name": "vecuronium", "type": "DRUG" }, { "name": "sevoflurane", "type": "DRUG" }, { "name": "desflurane", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "OrthoCarolina Research Institute, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 86, "start_date": "2016-09", "completion_date": "2019-06", "has_results": true, "last_update_posted_date": "2020-10-14", "last_synced_at": "2026-10-05T13:23:03.950Z", "location_count": 1, "location_summary": "Charlotte, North Carolina", "locations": [ { "city": "Charlotte", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03540030" }, { "nct_id": "NCT02312739", "title": "Nitrous Oxide for Pain Management During In-office Transcervical Sterilization", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Contraception", "Inhalation of Nitrous Oxide" ], "interventions": [ { "name": "In-office Transcervical Sterilization (Essure®)", "type": "PROCEDURE" }, { "name": "Standard Oral pain medications", "type": "DRUG" }, { "name": "Intramuscular Ketorolac", "type": "DRUG" }, { "name": "Placebo pills", "type": "DRUG" }, { "name": "Oxygen", "type": "OTHER" }, { "name": "Nitrous Oxide", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "DRUG", "OTHER" ], "sponsor": "University of New Mexico", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "FEMALE", "summary": "21 Years and older · Female only" }, "enrollment_count": 72, "start_date": "2014-02", "completion_date": "2015-03", "has_results": true, "last_update_posted_date": "2016-07-06", "last_synced_at": "2026-10-05T13:23:03.950Z", "location_count": 1, "location_summary": "Albuquerque, New Mexico", "locations": [ { "city": "Albuquerque", "state": "New Mexico" } ], "official_url": "https://clinicaltrials.gov/study/NCT02312739" }, { "nct_id": "NCT03367988", "title": "Opioid Free Anesthesia vs. Opioid Anesthesia Techniques.", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Analgesic Drug Dependence", "Colectomy" ], "interventions": [ { "name": "Opioid Anesthesia", "type": "DRUG" }, { "name": "Opioid-free Anesthesia", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of South Florida", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 100, "start_date": "2018-12-01", "completion_date": "2023-08", "has_results": false, "last_update_posted_date": "2022-05-25", "last_synced_at": "2026-10-05T13:23:03.950Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT03367988" }, { "nct_id": "NCT03913702", "title": "Subacromial Methylprednisolone Versus Ketorolac for Shoulder Impingement", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Subacromial Impingement", "Subacromial Impingement Syndrome" ], "interventions": [ { "name": "Ketorolac Tromethamine", "type": "DRUG" }, { "name": "Methylprednisolone Acetate", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "The University of Texas Medical Branch, Galveston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 1, "start_date": "2019-09-09", "completion_date": "2022-11-02", "has_results": true, "last_update_posted_date": "2025-01-03", "last_synced_at": "2026-10-05T13:23:03.950Z", "location_count": 1, "location_summary": "Galveston, Texas", "locations": [ { "city": "Galveston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03913702" }, { "nct_id": "NCT05017246", "title": "Comparing Intrathecal Morphine and Intraoperative Lidocaine Infusion to Epidural Anesthesia With Postoperative PCA for Patients Undergoing Exploratory Laparotomy", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Cancer Debulking", "Enlarged Uterus", "Fibroid Uterus", "Adnexal Mass" ], "interventions": [ { "name": "Bupivacaine", "type": "DRUG" }, { "name": "Morphine", "type": "DRUG" }, { "name": "Lidocaine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 110, "start_date": "2022-01-18", "completion_date": "2024-08-29", "has_results": true, "last_update_posted_date": "2025-07-31", "last_synced_at": "2026-10-05T13:23:03.950Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT05017246" }, { "nct_id": "NCT07682662", "title": "Low Dose Bolus Ketamine For Use In Sickle Cell Pain Crisis", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Vaso-Occlusive Pain Episode in Sickle Cell Disease", "Sickle Cell Disease (SCD)" ], "interventions": [ { "name": "Standardized Low-dose bolus IV Ketamine within 30 minutes of arrival and every 1 hour as needed for max of 3 doses.", "type": "DRUG" }, { "name": "Standard Care (in control arm)", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "University of Mississippi Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "2 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "2 Years to 21 Years" }, "enrollment_count": 400, "start_date": "2026-08-01", "completion_date": "2029-10-01", "has_results": false, "last_update_posted_date": "2026-07-06", "last_synced_at": "2026-10-05T13:23:03.950Z", "location_count": 1, "location_summary": "Jackson, Mississippi", "locations": [ { "city": "Jackson", "state": "Mississippi" } ], "official_url": "https://clinicaltrials.gov/study/NCT07682662" }, { "nct_id": "NCT02958566", "title": "Multimodal Narcotic Limited Perioperative Pain Control With Colorectal Surgery", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Colon Cancer", "Colon Diverticulosis", "Colonic Neoplasms", "Colonic Diverticulitis", "Pain, Postoperative", "Ileus", "Ileus Paralytic", "Ileus; Mechanical", "Constipation Drug Induced", "Constipation", "Rectum Cancer", "Rectum Neoplasm" ], "interventions": [ { "name": "Acetaminophen", "type": "DRUG" }, { "name": "Gabapentin", "type": "DRUG" }, { "name": "Orphenadrine", "type": "DRUG" }, { "name": "Lidocaine", "type": "DRUG" }, { "name": "Marcaine", "type": "DRUG" }, { "name": "Ketamine", "type": "DRUG" }, { "name": "Methadone", "type": "DRUG" }, { "name": "Tramadol", "type": "DRUG" }, { "name": "Ketorolac", "type": "DRUG" }, { "name": "Morphine Sulfate", "type": "DRUG" }, { "name": "Fentanyl", "type": "DRUG" }, { "name": "Dilaudid", "type": "DRUG" }, { "name": "Hydrocodone-Acetaminophen Tab 5-325 MG", "type": "DRUG" }, { "name": "HYDROCODONE/ACETAMINOPHEN 5 Mg-325 Mg ORAL TABLET", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Illinois College of Medicine at Peoria", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 80, "start_date": "2017-01", "completion_date": "2018-12", "has_results": false, "last_update_posted_date": "2017-03-20", "last_synced_at": "2026-10-05T13:23:03.950Z", "location_count": 1, "location_summary": "Peoria, Illinois", "locations": [ { "city": "Peoria", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT02958566" }, { "nct_id": "NCT06189781", "title": "Pain Injection Versus Epidural Anesthesia for Hip Surgery in Pediatric Patients With Cerebral Palsy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Cerebral Palsy", "Hip Dysplasia", "Pain, Postoperative" ], "interventions": [ { "name": "Ropivacaine injection", "type": "DRUG" }, { "name": "Bupivacaine, lidocaine, ropivacaine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "18 Years", "sex": "ALL", "summary": "Up to 18 Years" }, "enrollment_count": 90, "start_date": "2023-12-01", "completion_date": "2027-06-30", "has_results": false, "last_update_posted_date": "2024-06-11", "last_synced_at": "2026-10-05T13:23:03.950Z", "location_count": 4, "location_summary": "Los Angeles, California • Santa Monica, California • Chicago, Illinois", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Santa Monica", "state": "California" }, { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06189781" }, { "nct_id": "NCT03319784", "title": "Analysis for NSAID VS Corticosteroid Shoulder Injection in Diabetic Patients", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Rotator Cuff Tear", "Rotator Cuff Injury", "Rotator Cuff Tendinitis", "Diabetes Mellitus" ], "interventions": [ { "name": "Ketorolac", "type": "DRUG" }, { "name": "Triamcinolone Acetonide", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Milton S. Hershey 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": 0, "start_date": "2018-09-05", "completion_date": "2020-10-05", "has_results": false, "last_update_posted_date": "2019-02-15", "last_synced_at": "2026-10-05T13:23:03.950Z", "location_count": 1, "location_summary": "Hershey, Pennsylvania", "locations": [ { "city": "Hershey", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03319784" }, { "nct_id": "NCT00617097", "title": "Paracervical Block in First Trimester Surgical Abortions", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Pain", "Surgical Abortion" ], "interventions": [ { "name": "lidocaine", "type": "DRUG" }, { "name": "ketorolac and lidocaine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "FEMALE", "summary": "18 Years to 50 Years · Female only" }, "enrollment_count": 50, "start_date": "2008-01", "completion_date": "2009-06", "has_results": true, "last_update_posted_date": "2017-09-15", "last_synced_at": "2026-10-05T13:23:03.950Z", "location_count": 1, "location_summary": "Portland, Oregon", "locations": [ { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT00617097" } ] }