{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Lidocaine+alone", "query": { "intervention": "Lidocaine alone" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 207, "total_pages": 21, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Lidocaine+alone&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-12T22:04:23.710Z", "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": "NCT03543033", "title": "Preoperative Corticosteroid Epidural Injection and Lumbar Decompression Surgery Outcomes", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lumbar Radiculopathy" ], "interventions": [ { "name": "Corticosteroid injection", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Lahey Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "30 Years to 75 Years" }, "enrollment_count": 0, "start_date": "2018-09-10", "completion_date": "2020-05-01", "has_results": false, "last_update_posted_date": "2020-06-18", "last_synced_at": "2026-09-12T22:04:23.710Z", "location_count": 1, "location_summary": "Burlington, Massachusetts", "locations": [ { "city": "Burlington", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03543033" }, { "nct_id": "NCT07630155", "title": "Office-Based Ureteroscopy Utilizing a Single Use Digital, Flexible Ureteroscope for Upper Tract Urothelial Carcinoma", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Renal Pelvis and Ureter Urothelial Carcinoma" ], "interventions": [ { "name": "Analgesic Agent", "type": "DRUG" }, { "name": "Electronic Health Record Review", "type": "OTHER" }, { "name": "Lidocaine Topical", "type": "DRUG" }, { "name": "Medical Device Usage and Evaluation", "type": "DEVICE" }, { "name": "Survey Administration", "type": "OTHER" }, { "name": "Ureteroscopy", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "OTHER", "DEVICE", "PROCEDURE" ], "sponsor": "University of Michigan Rogel Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 10, "start_date": "2026-08", "completion_date": "2027-08", "has_results": false, "last_update_posted_date": "2026-07-10", "last_synced_at": "2026-09-12T22:04:23.710Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT07630155" }, { "nct_id": "NCT06999057", "title": "Quadriceps Motor Unit Adaptation to Simulated Knee Injury", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Muscle Inhibition", "Knee Injury Simulation" ], "interventions": [ { "name": "Joint Effusion via 60 mL Sterile Saline", "type": "DEVICE" }, { "name": "Intra-articular Lidocaine", "type": "DRUG" }, { "name": "Sham injection", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "DRUG", "OTHER" ], "sponsor": "University of Central Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "30 Years", "sex": "ALL", "summary": "18 Years to 30 Years" }, "enrollment_count": 45, "start_date": "2026-08-01", "completion_date": "2027-08-01", "has_results": false, "last_update_posted_date": "2026-05-01", "last_synced_at": "2026-09-12T22:04:23.710Z", "location_count": 1, "location_summary": "Orlando, Florida", "locations": [ { "city": "Orlando", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06999057" }, { "nct_id": "NCT00841386", "title": "Treatment of Keratoconus Using Collagen Cross-Linking", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Keratoconus" ], "interventions": [ { "name": "Riboflavin-5-phosphate", "type": "DRUG" }, { "name": "Sham cross-linking", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University at Buffalo", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "16 Years", "maximum_age": "35 Years", "sex": "ALL", "summary": "16 Years to 35 Years" }, "enrollment_count": 150, "start_date": "2008-09", "completion_date": "2011-12", "has_results": false, "last_update_posted_date": "2009-02-11", "last_synced_at": "2026-09-12T22:04:23.710Z", "location_count": 2, "location_summary": "Amherst, New York • Buffalo, New York", "locations": [ { "city": "Amherst", "state": "New York" }, { "city": "Buffalo", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00841386" }, { "nct_id": "NCT04766996", "title": "PROUD Study - Preventing Opioid Use Disorders", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Anesthesia", "Opioid Use" ], "interventions": [ { "name": "Guided mindfulness exercises", "type": "BEHAVIORAL" }, { "name": "Self-administered aromatherapy", "type": "OTHER" }, { "name": "Baby aspirin", "type": "DRUG" }, { "name": "Tylenol/Acetaminophen", "type": "DRUG" }, { "name": "Pregabalin", "type": "DRUG" }, { "name": "Prednisone", "type": "DRUG" }, { "name": "Meloxicam", "type": "DRUG" }, { "name": "Prilosec", "type": "DRUG" }, { "name": "Tramadol", "type": "DRUG" }, { "name": "Voltaren", "type": "DRUG" }, { "name": "Zofran", "type": "DRUG" }, { "name": "Pepcid", "type": "DRUG" }, { "name": "Reglan", "type": "DRUG" }, { "name": "Versed", "type": "DRUG" }, { "name": "Lidocaine", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" }, { "name": "Ancef", "type": "DRUG" }, { "name": "Tranexamic Acid (TXA)", "type": "DRUG" }, { "name": "Decadron", "type": "DRUG" }, { "name": "Bupivacaine hydrochloride", "type": "DRUG" }, { "name": "Toradol", "type": "DRUG" } ], "intervention_types": [ "BEHAVIORAL", "OTHER", "DRUG" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 57, "start_date": "2021-05-17", "completion_date": "2021-12-27", "has_results": true, "last_update_posted_date": "2023-06-22", "last_synced_at": "2026-09-12T22:04:23.710Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT04766996" }, { "nct_id": "NCT07369128", "title": "Propofol-Only Versus Dexmedetomidine-Propofol in Children Undergoing Magnetic Resonance Imaging", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "MRI Sedation", "Pediatric Sedation", "Propofol Dosage", "Emergence Delirium, Anesthesia", "Recovery Time", "Dexmedetomidine" ], "interventions": [ { "name": "Dexmedetomidine (IV) 0.5 mcg/kg", "type": "DRUG" }, { "name": "Propofol (IV) 2-4 mg/kg", "type": "DRUG" }, { "name": "Dexmedetomidine (IV) 1 mcg/kg", "type": "DRUG" }, { "name": "Propofol (IV) 1-2 mg/kg", "type": "DRUG" }, { "name": "Propofol (IV) Infusion 250 mcg/kg/min", "type": "DRUG" }, { "name": "Propofol (IV) Infusion 150 mcg/kg/min", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Boston Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Year", "maximum_age": "12 Years", "sex": "ALL", "summary": "1 Year to 12 Years" }, "enrollment_count": 105, "start_date": "2026-06", "completion_date": "2028-03", "has_results": false, "last_update_posted_date": "2026-05-29", "last_synced_at": "2026-09-12T22:04:23.710Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07369128" }, { "nct_id": "NCT04203225", "title": "Comparison of Two Application Techniques for LET Gel", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Lacerations", "Pain, Procedural", "LET" ], "interventions": [ { "name": "LET Lidocaine (4%), Epinephrine (0.1%), and Tetracaine (0.5%) topical gel", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "7 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "7 Years to 17 Years" }, "enrollment_count": 48, "start_date": "2017-05-22", "completion_date": "2019-11-12", "has_results": true, "last_update_posted_date": "2021-02-18", "last_synced_at": "2026-09-12T22:04:23.710Z", "location_count": 2, "location_summary": "Orange, California • Torrance, California", "locations": [ { "city": "Orange", "state": "California" }, { "city": "Torrance", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04203225" }, { "nct_id": "NCT06533345", "title": "VCOM Pain Free Research Collaborative", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Pain" ], "interventions": [ { "name": "Behavior Change Coaching", "type": "BEHAVIORAL" }, { "name": "Nutrition", "type": "BEHAVIORAL" }, { "name": "Autonomic Recalibration", "type": "OTHER" }, { "name": "Dry Needling", "type": "PROCEDURE" }, { "name": "Osteopathic Manipulative Treatment", "type": "OTHER" }, { "name": "Counseling Psychology", "type": "BEHAVIORAL" }, { "name": "Multiple Treatments", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER", "PROCEDURE" ], "sponsor": "Edward Via Virginia College of Osteopathic Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "21 Years to 80 Years" }, "enrollment_count": 120, "start_date": "2024-08-30", "completion_date": "2027-08-01", "has_results": false, "last_update_posted_date": "2026-02-20", "last_synced_at": "2026-09-12T22:04:23.710Z", "location_count": 1, "location_summary": "Auburn, Alabama", "locations": [ { "city": "Auburn", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT06533345" }, { "nct_id": "NCT00203294", "title": "A Research Study to Examine the Difference Between Local Anesthetics Alone and Local Anesthetics Plus Steroids in the Treatment of Chronic Headache", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Migraine" ], "interventions": [ { "name": "lidocaine, bupivicaine and saline", "type": "DRUG" }, { "name": "lidocaine plus bupivicaine plus triamcinolone (steroid)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Thomas Jefferson University", "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": 45, "start_date": "2005-06", "completion_date": "2006-06", "has_results": true, "last_update_posted_date": "2014-05-07", "last_synced_at": "2026-09-12T22:04:23.710Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00203294" }, { "nct_id": "NCT03913845", "title": "The Impact of Retropubic Lidocaine vs Saline on Postoperative Urinary Retention Following Midurethral Sling", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Stress Urinary Incontinence" ], "interventions": [ { "name": "lidocaine with epinephrine", "type": "DRUG" }, { "name": "Normal saline with epinephrine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "West Penn Allegheny Health System", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "FEMALE", "summary": "18 Years to 99 Years · Female only" }, "enrollment_count": 150, "start_date": "2019-11-25", "completion_date": "2024-11-14", "has_results": true, "last_update_posted_date": "2026-04-30", "last_synced_at": "2026-09-12T22:04:23.710Z", "location_count": 4, "location_summary": "Bethel Park, Pennsylvania • Jefferson Hills, Pennsylvania • Pittsburgh, Pennsylvania + 1 more", "locations": [ { "city": "Bethel Park", "state": "Pennsylvania" }, { "city": "Jefferson Hills", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Wexford", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03913845" } ] }