{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Ketorolac+60+Mg", "query": { "intervention": "Ketorolac 60 Mg" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 14, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Ketorolac+60+Mg&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-28T08:36:11.776Z", "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": "NCT05248984", "title": "Dosing of Ketorolac Impacts Post-cesarean paiN manaGemenet (KING)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Post Cesarean Pain" ], "interventions": [ { "name": "Ketorolac 30 Mg", "type": "DRUG" }, { "name": "Ketorolac 60 Mg", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "18 Years to 45 Years · Female only" }, "enrollment_count": 92, "start_date": "2022-06-08", "completion_date": "2023-11-30", "has_results": true, "last_update_posted_date": "2026-02-25", "last_synced_at": "2026-09-28T08:36:11.776Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05248984" }, { "nct_id": "NCT05324358", "title": "Ketorolac Applied by Continuous IV Infusion for Treatment of Moderately Severe Postoperative Pain Following Bunionectomy", "overall_status": "SUSPENDED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Pain, Postoperative" ], "interventions": [ { "name": "Ketorolac Tromethamine", "type": "DRUG" }, { "name": "Morphine Sulfate", "type": "DRUG" }, { "name": "Intravenous Placebo for NTM-001", "type": "OTHER" }, { "name": "IV Placebo for Morphine", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Neumentum, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "18 Years to 64 Years" }, "enrollment_count": 341, "start_date": "2022-12-14", "completion_date": "2027-05", "has_results": false, "last_update_posted_date": "2026-04-23", "last_synced_at": "2026-09-28T08:36:11.776Z", "location_count": 10, "location_summary": "Sun City, Arizona • Bakersfield, California • Canoga Park, California + 7 more", "locations": [ { "city": "Sun City", "state": "Arizona" }, { "city": "Bakersfield", "state": "California" }, { "city": "Canoga Park", "state": "California" }, { "city": "Pomona", "state": "California" }, { "city": "Overland Park", "state": "Kansas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05324358" }, { "nct_id": "NCT06994442", "title": "Optimizing Pain Treatment in Children On Mechanical Ventilation", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Mechanical Ventilation", "Pediatric Acute Respiratory Failure", "Analgesics, Opioid", "Sedation and Analgesia" ], "interventions": [ { "name": "Acetaminophen", "type": "DRUG" }, { "name": "Ketorolac", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Weill Medical College of Cornell University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "2 Months", "maximum_age": "17 Years", "sex": "ALL", "summary": "2 Months to 17 Years" }, "enrollment_count": 644, "start_date": "2025-12-29", "completion_date": "2029-08-31", "has_results": false, "last_update_posted_date": "2026-07-30", "last_synced_at": "2026-09-28T08:36:11.776Z", "location_count": 16, "location_summary": "Little Rock, Arkansas • Washington D.C., District of Columbia • Ann Arbor, Michigan + 13 more", "locations": [ { "city": "Little Rock", "state": "Arkansas" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Ann Arbor", "state": "Michigan" }, { "city": "Detroit", "state": "Michigan" }, { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT06994442" }, { "nct_id": "NCT03513770", "title": "Autonomic Control of the Circulation and VDR", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Venous Distension Reflex", "Blood Pressure" ], "interventions": [ { "name": "Wrist-to-elbow (W-E) occlusion", "type": "OTHER" }, { "name": "ketorolac tromethamine", "type": "DRUG" }, { "name": "saline control", "type": "DRUG" } ], "intervention_types": [ "OTHER", "DRUG" ], "sponsor": "Milton S. Hershey Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": "35 Years", "sex": "ALL", "summary": "21 Years to 35 Years" }, "enrollment_count": 18, "start_date": "2019-08-14", "completion_date": "2027-11-01", "has_results": false, "last_update_posted_date": "2026-07-09", "last_synced_at": "2026-09-28T08:36:11.776Z", "location_count": 1, "location_summary": "Hershey, Pennsylvania", "locations": [ { "city": "Hershey", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03513770" }, { "nct_id": "NCT07435077", "title": "Examining Analgesic Synergy and Efficacy in Trauma Care", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Opioid Use Disorder" ], "interventions": [ { "name": "Buprenorphine", "type": "DRUG" }, { "name": "Oxycodone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Wake Forest University Health Sciences", "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": 282, "start_date": "2026-10", "completion_date": "2027-02", "has_results": false, "last_update_posted_date": "2026-08-28", "last_synced_at": "2026-09-28T08:36:11.776Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT07435077" }, { "nct_id": "NCT03823534", "title": "Post-Op Pain Control for Prophylactic Intramedullary Nailing.", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Bone Metastases", "Lymphoma", "Multiple Myeloma", "Opioid Use", "Pain" ], "interventions": [ { "name": "Ketorolac", "type": "DRUG" }, { "name": "Normal saline", "type": "DRUG" }, { "name": "Acetaminophen", "type": "DRUG" }, { "name": "Oxycodone Acetaminophen", "type": "DRUG" }, { "name": "Morphine", "type": "DRUG" }, { "name": "Hydrocodone/Acetaminophen", "type": "DRUG" }, { "name": "Oxycodone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "St. Louis University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2019-02-20", "completion_date": "2027-03-31", "has_results": false, "last_update_posted_date": "2026-04-22", "last_synced_at": "2026-09-28T08:36:11.776Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT03823534" }, { "nct_id": "NCT02664116", "title": "IM Ketorolac vs Cambia for the Acute Treatment of Severe Migraine", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Migraine Headache" ], "interventions": [ { "name": "Diclofenac postassium powder for oral solution and placebo injection", "type": "DRUG" }, { "name": "Ketorolac intramuscular injection and placebo oral solution", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Scripps Health", "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": 40, "start_date": "2016-01", "completion_date": "2017-07", "has_results": false, "last_update_posted_date": "2016-02-03", "last_synced_at": "2026-09-28T08:36:11.776Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02664116" }, { "nct_id": "NCT01595282", "title": "Intramuscular Ketorolac Versus Oral Ibuprofen for Pain Relief in First Trimester Suction Curettage", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pain" ], "interventions": [ { "name": "Ketorolac", "type": "DRUG" }, { "name": "Ibuprofen", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Planned Parenthood League of Massachusetts", "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": 94, "start_date": "2011-06", "completion_date": "2012-06", "has_results": true, "last_update_posted_date": "2014-07-02", "last_synced_at": "2026-09-28T08:36:11.776Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01595282" }, { "nct_id": "NCT04763876", "title": "Intramuscular Ketorolac at Two Single-Dose Regimens", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Musculoskeletal Pain", "Analgesia", "Adverse Event" ], "interventions": [ { "name": "Ketorolac Injection 15 mg", "type": "DRUG" }, { "name": "Ketorolac Injection 60 mg", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "William Beaumont Army Medical Center", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "18 Years to 55 Years" }, "enrollment_count": 110, "start_date": "2020-06-27", "completion_date": "2021-02-04", "has_results": true, "last_update_posted_date": "2025-10-15", "last_synced_at": "2026-09-28T08:36:11.776Z", "location_count": 1, "location_summary": "El Paso, Texas", "locations": [ { "city": "El Paso", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04763876" }, { "nct_id": "NCT04704297", "title": "Trigger Point Injection for Myofascial Pain Syndrome in the Low Back: A Randomized Controlled Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Low Back Pain", "Myofascial Pain Syndrome Lower Back" ], "interventions": [ { "name": "Treatment of Myofascial Pain Syndrome in the low back. This intervention will be based on outcomes of the medications listed below.", "type": "DRUG" }, { "name": "Evaluation of functional ability using a patient centered functional score known as the Modified Oswestry Disability Index (MODI). The intervention will be based on outcomes of medications below.", "type": "DRUG" }, { "name": "Following up with participants 60-72 hours after treatment in the Emergency Department. This intervention will be based on outcomes of the medications listed below.", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Madigan Army Medical Center", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 180, "start_date": "2020-12-28", "completion_date": "2022-07-01", "has_results": false, "last_update_posted_date": "2021-01-12", "last_synced_at": "2026-09-28T08:36:11.776Z", "location_count": 1, "location_summary": "Tacoma, Washington", "locations": [ { "city": "Tacoma", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT04704297" } ] }