{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Advil&page=19", "query": { "intervention": "Advil", "page": 19 }, "page_size": 10 }, "pagination": { "page": 19, "page_size": 10, "total_count": 434, "total_pages": 44, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Advil&page=20&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Advil&page=18&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-24T01:30:02.506Z", "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": "NCT02588027", "title": "Effect of Ibuprofen on Postoperative Opiate Medication Use and Shoulder Functional Outcomes", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Rotator Cuff Tear Arthropathy" ], "interventions": [ { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 110, "start_date": "2015-10", "completion_date": "2022-09", "has_results": true, "last_update_posted_date": "2024-12-06", "last_synced_at": "2026-10-24T01:30:02.506Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02588027" }, { "nct_id": "NCT06603662", "title": "Systemic Oral Glucocorticoids for the Treatment of Acute Osteoarthritis Pain in the Emergency Department", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Osteoarthritis", "Osteoarthritis (OA) of the Knee", "Osteoarthritis (OA) of the Shoulder", "Osteoarthritis (OA) of the Hip" ], "interventions": [ { "name": "Prednisone", "type": "DRUG" }, { "name": "Dexamethasone", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "WellSpan Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 192, "start_date": "2025-02-24", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2026-08-19", "last_synced_at": "2026-10-24T01:30:02.506Z", "location_count": 1, "location_summary": "York, Pennsylvania", "locations": [ { "city": "York", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06603662" }, { "nct_id": "NCT00951561", "title": "A Comparison Study of Pain Relief From Dysmenorrhea Between the Vipon Tampon and Ibuprofen", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Dysmenorrhea" ], "interventions": [ { "name": "Vipon", "type": "DEVICE" }, { "name": "Ibuprofen", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "DRUG" ], "sponsor": "Another Way Products", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 115, "start_date": "2006-11", "completion_date": "2009-09", "has_results": true, "last_update_posted_date": "2011-06-16", "last_synced_at": "2026-10-24T01:30:02.506Z", "location_count": 2, "location_summary": "Kansas City, Missouri", "locations": [ { "city": "Kansas City", "state": "Missouri" }, { "city": "Kansas City", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT00951561" }, { "nct_id": "NCT03493945", "title": "Phase I/II Study of Immunotherapy Combination BN-Brachyury Vaccine, M7824, N-803 and Epacadostat (QuEST1)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Metastatic Castration-resistant Prostate Cancer", "Prostate Cancer", "Prostate Neoplasm", "Advanced Solid Tumor", "Solid Tumor", "Non-metastatic Castration-resistant Prostate Cancer" ], "interventions": [ { "name": "M7824", "type": "BIOLOGICAL" }, { "name": "N-803", "type": "DRUG" }, { "name": "MVA-BN-Brachyury", "type": "BIOLOGICAL" }, { "name": "FPV-Brachyury", "type": "BIOLOGICAL" }, { "name": "Epacadostat", "type": "DRUG" }, { "name": "Acetaminophen", "type": "DRUG" }, { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Naproxen", "type": "DRUG" }, { "name": "Benadryl", "type": "OTHER" }, { "name": "EKG", "type": "DIAGNOSTIC_TEST" }, { "name": "Bone scan", "type": "DIAGNOSTIC_TEST" }, { "name": "CT chest, abdomen and pelvis", "type": "DIAGNOSTIC_TEST" }, { "name": "MRI", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "BIOLOGICAL", "DRUG", "OTHER", "DIAGNOSTIC_TEST" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "18 Years to 120 Years" }, "enrollment_count": 59, "start_date": "2018-05-01", "completion_date": "2024-10-08", "has_results": true, "last_update_posted_date": "2025-09-30", "last_synced_at": "2026-10-24T01:30:02.506Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT03493945" }, { "nct_id": "NCT06484439", "title": "Controlled Trial to Determine Most Effective Post-Operative Analgesia After Third Molar Extraction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Pain, Post-operative", "Third Molar", "Oral Surgery", "Pain, Acute" ], "interventions": [ { "name": "Ketorolac", "type": "DRUG" }, { "name": "Oxycodone", "type": "DRUG" }, { "name": "Acetaminophen", "type": "DRUG" }, { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Hydrocodone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "United States Naval Medical Center, San Diego", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "44 Years", "sex": "ALL", "summary": "18 Years to 44 Years" }, "enrollment_count": 80, "start_date": "2018-02-14", "completion_date": "2021-12-01", "has_results": false, "last_update_posted_date": "2024-07-10", "last_synced_at": "2026-10-24T01:30:02.506Z", "location_count": 1, "location_summary": "San Diego, California", "locations": [ { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06484439" }, { "nct_id": "NCT01974609", "title": "Narcotic vs. Non-narcotic Pain Study Protocol", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Carpal Tunnel" ], "interventions": [ { "name": "Narcotic", "type": "DRUG" }, { "name": "non-narcotic", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Horizon Health Network", "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": 347, "start_date": "2016-03", "completion_date": "2022-02-24", "has_results": false, "last_update_posted_date": "2022-03-11", "last_synced_at": "2026-10-24T01:30:02.506Z", "location_count": 3, "location_summary": "Philadelphia, Pennsylvania • Sioux Falls, South Dakota • Roanoke, Virginia", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" }, { "city": "Sioux Falls", "state": "South Dakota" }, { "city": "Roanoke", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01974609" }, { "nct_id": "NCT00346216", "title": "Prospective Randomized Evaluation Of Celecoxib Integrated Safety Vs Ibuprofen Or Naproxen", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Arthritis, Rheumatoid" ], "interventions": [ { "name": "celecoxib", "type": "DRUG" }, { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Naproxen", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Pfizer's Upjohn has merged with Mylan to form Viatris Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 24081, "start_date": "2006-10-04", "completion_date": "2016-04-12", "has_results": true, "last_update_posted_date": "2021-03-03", "last_synced_at": "2026-10-24T01:30:02.506Z", "location_count": 871, "location_summary": "Alabaster, Alabama • Bessemer, Alabama • Birmingham, Alabama + 515 more", "locations": [ { "city": "Alabaster", "state": "Alabama" }, { "city": "Bessemer", "state": "Alabama" }, { "city": "Birmingham", "state": "Alabama" }, { "city": "Birmingham", "state": "Alabama" }, { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT00346216" }, { "nct_id": "NCT00890604", "title": "Outcomes Associated With Application of a Normothermia Protocol in Patients With Severe Neurological Insult and Fever", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Subarachnoid Hemorrhage", "Severe Traumatic Brain Injury" ], "interventions": [ { "name": "Stepwise normothermia protocol", "type": "OTHER" }, { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Acetominophen", "type": "DRUG" } ], "intervention_types": [ "OTHER", "DRUG" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 10, "start_date": "2009-07", "completion_date": "2011-07", "has_results": false, "last_update_posted_date": "2024-01-30", "last_synced_at": "2026-10-24T01:30:02.506Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT00890604" }, { "nct_id": "NCT03604341", "title": "Cannabinoids for Pain Control During Medical Abortion", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Medical Abortion", "Pain" ], "interventions": [ { "name": "Dronabinol 5mg Cap", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Oregon Health and Science University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "89 Years", "sex": "FEMALE", "summary": "21 Years to 89 Years · Female only" }, "enrollment_count": 72, "start_date": "2018-11-01", "completion_date": "2019-05-28", "has_results": true, "last_update_posted_date": "2020-04-07", "last_synced_at": "2026-10-24T01:30:02.506Z", "location_count": 1, "location_summary": "Portland, Oregon", "locations": [ { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT03604341" }, { "nct_id": "NCT02807623", "title": "Do NSAIDS or Executing Exercise Decrease Local Erythema, Site Swelling & Pain After INoculation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Immune System and Related Disorders" ], "interventions": [ { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Compound Exercise of Push-ups", "type": "BEHAVIORAL" }, { "name": "oral placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG", "BEHAVIORAL" ], "sponsor": "Womack 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": 300, "start_date": "2016-09", "completion_date": "2018-12", "has_results": true, "last_update_posted_date": "2020-11-27", "last_synced_at": "2026-10-24T01:30:02.506Z", "location_count": 2, "location_summary": "Bethesda, Maryland • Fort Bragg, North Carolina", "locations": [ { "city": "Bethesda", "state": "Maryland" }, { "city": "Fort Bragg", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT02807623" } ] }