{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Placebo+%28for+racemic+epinephrine%29", "query": { "intervention": "Placebo (for racemic epinephrine)" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 61, "total_pages": 7, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Placebo+%28for+racemic+epinephrine%29&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-10-01T20:42:36.165Z", "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": "NCT02007434", "title": "Patient Experience Study of Deoxycholic Acid Injection", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Moderate or Severe Submental Fullness" ], "interventions": [ { "name": "Deoxycholic Acid Injection", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Cold Compress", "type": "OTHER" }, { "name": "Lidocaine / Epinephrine", "type": "DRUG" }, { "name": "Loratadine", "type": "DRUG" }, { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Compression Chin Strap", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Kythera Biopharmaceuticals", "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": 84, "start_date": "2013-12", "completion_date": "2014-06", "has_results": true, "last_update_posted_date": "2015-07-28", "last_synced_at": "2026-10-01T20:42:36.165Z", "location_count": 1, "location_summary": "Tempe, Arizona", "locations": [ { "city": "Tempe", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT02007434" }, { "nct_id": "NCT00002659", "title": "Cisplatin Plus Epinephrine in Treating Patients With Recurrent or Refractory Head and Neck Cancer", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Head and Neck Cancer" ], "interventions": [ { "name": "cisplatin-e therapeutic implant", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Matrix Pharmaceutical", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "1995-05", "completion_date": null, "has_results": false, "last_update_posted_date": "2013-12-19", "last_synced_at": "2026-10-01T20:42:36.165Z", "location_count": 26, "location_summary": "Tucson, Arizona • Los Angeles, California • Palo Alto, California + 21 more", "locations": [ { "city": "Tucson", "state": "Arizona" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Los Angeles", "state": "California" }, { "city": "Palo Alto", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00002659" }, { "nct_id": "NCT04814433", "title": "Evaluating Postoperative Non-Opioid Pain Management Utilizing Local Anesthetics Coupled With Modulated Coagulation", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Opioid Pain Medication" ], "interventions": [ { "name": "Tranexamic acid", "type": "DRUG" }, { "name": "Aminocaproic acid", "type": "DRUG" }, { "name": "Recombinant Human Thrombin", "type": "DRUG" }, { "name": "Lidocaine Hydrochloride with Epinephrine", "type": "DRUG" }, { "name": "Bupivacaine Hydrochloride with Epinephrine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 46, "start_date": "2021-03-24", "completion_date": "2023-07-10", "has_results": true, "last_update_posted_date": "2024-06-26", "last_synced_at": "2026-10-01T20:42:36.165Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04814433" }, { "nct_id": "NCT02230735", "title": "Bupivacaine Injections Into Uterosacral Ligaments During Robotic Assisted Total Hysterectomies", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pain" ], "interventions": [ { "name": "Bipivacaine 0.5% with epinephrine", "type": "DRUG" }, { "name": "Normal Saline", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Souza, Amanda, M.D.", "sponsor_class": "INDIV", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "21 Years to 65 Years · Female only" }, "enrollment_count": 0, "start_date": "2014-08", "completion_date": "2014-08", "has_results": false, "last_update_posted_date": "2016-05-05", "last_synced_at": "2026-10-01T20:42:36.165Z", "location_count": 1, "location_summary": "Farmington Hills, Michigan", "locations": [ { "city": "Farmington Hills", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT02230735" }, { "nct_id": "NCT05029726", "title": "Regional Anesthesia in Minimally Invasive Lumbar Spine Surgery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Lumbar Spinal Stenosis", "Lumbar Disc Herniation", "Lumbar Spondylolisthesis", "Lumbar Spondylosis", "Lumbar Radiculopathy", "Lumbar Spine Instability", "Synovial Cyst", "Degenerative Disc Disease", "Degenerative Spondylolisthesis", "Degenerative Intervertebral Discs" ], "interventions": [ { "name": "Bupivacaine-Epinephrine 0.25%-1:200,000 Injectable Solution plus clonidine", "type": "DRUG" }, { "name": "normal saline", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "John O'Toole", "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": 125, "start_date": "2022-02-01", "completion_date": "2027-04-30", "has_results": false, "last_update_posted_date": "2026-02-17", "last_synced_at": "2026-10-01T20:42:36.165Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05029726" }, { "nct_id": "NCT00578214", "title": "Safety and Efficacy of Oral Midazolam for Perioperative Anxiety Relief of Patients Undergoing Mohs Micrographic Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Basal Cell Carcinoma", "Squamous Cell Carcinoma", "Skin Cancer", "Anxiety" ], "interventions": [ { "name": "Randomized Midazolam", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" }, { "name": "Local Anesthesia", "type": "DRUG" }, { "name": "Prospective Midazolam", "type": "DRUG" } ], "intervention_types": [ "DRUG", "OTHER" ], "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": 75, "start_date": "2007-03", "completion_date": "2008-06", "has_results": true, "last_update_posted_date": "2012-02-09", "last_synced_at": "2026-10-01T20:42:36.165Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT00578214" }, { "nct_id": "NCT06447194", "title": "Effect of RECK in Posterior Spinal Fusion", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Degenerative Lumbar Spinal Stenosis", "Degenerative Disc Disease", "Degenerative Spondylolisthesis", "Degenerative Disease" ], "interventions": [ { "name": "Ropivacaine, Epinephrine, Clonidine, and Ketorolac Injection Cocktail", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "University of Maryland, Baltimore", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "88 Years", "sex": "ALL", "summary": "18 Years to 88 Years" }, "enrollment_count": 0, "start_date": "2025-10-01", "completion_date": "2027-04-01", "has_results": false, "last_update_posted_date": "2025-07-31", "last_synced_at": "2026-10-01T20:42:36.165Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT06447194" }, { "nct_id": "NCT00720330", "title": "Lidocaine and Ketamine Versus Standard Care on Acute and Chronic Pain", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pain", "Nausea" ], "interventions": [ { "name": "ropivacaine", "type": "DRUG" }, { "name": "Lidocaine/Ketamine", "type": "DRUG" }, { "name": "placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "MALE", "summary": "18 Years to 75 Years · Male only" }, "enrollment_count": 12, "start_date": "2008-07", "completion_date": "2010-02", "has_results": true, "last_update_posted_date": "2019-03-12", "last_synced_at": "2026-10-01T20:42:36.165Z", "location_count": 1, "location_summary": "Mayfield Heights, Ohio", "locations": [ { "city": "Mayfield Heights", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT00720330" }, { "nct_id": "NCT01997567", "title": "Preemptive Femoral & Lateral Femoral Cutaneous Nerve Blocks for THA Acute Pain", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Internal Derangement of Hip", "Acetabular Labrum Tear" ], "interventions": [ { "name": "Ropivacaine", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Rush University 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": 3, "start_date": "2013-07", "completion_date": "2014-03", "has_results": true, "last_update_posted_date": "2018-10-03", "last_synced_at": "2026-10-01T20:42:36.165Z", "location_count": 1, "location_summary": "Oak Park, Illinois", "locations": [ { "city": "Oak Park", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT01997567" }, { "nct_id": "NCT07213635", "title": "Paracervical Injection and Opioid Use After Vaginal Hysterectomy for Prolapse", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Opioid Use", "Surgical Recovery", "Vaginal Hysterectomy", "Prolapse Pelvic", "Postoperative Pain" ], "interventions": [ { "name": "Bupivacaine-epinephrine", "type": "DRUG" }, { "name": "Normal saline", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of North Carolina, Chapel Hill", "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": 56, "start_date": "2025-10-20", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-08-21", "last_synced_at": "2026-10-01T20:42:36.165Z", "location_count": 1, "location_summary": "Raleigh, North Carolina", "locations": [ { "city": "Raleigh", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT07213635" } ] }