{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Mandibular+Surgery", "query": { "condition": "Mandibular Surgery" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 20, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Mandibular+Surgery&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-05-22T05:17:57.856Z", "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": "NCT04283981", "title": "Comparison of Operating Room Time Length With the Use of Virtual Surgical Planning Versus Conventional Treatment of Mandible Fractures", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mandibular Fractures" ], "interventions": [ { "name": "Control group without use of VSP", "type": "DEVICE" }, { "name": "Treatment Group with use of VSP", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "The University of Texas Health Science Center, Houston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 28, "start_date": "2021-01-24", "completion_date": "2022-11-10", "has_results": true, "last_update_posted_date": "2024-06-20", "last_synced_at": "2026-05-22T05:17:57.856Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04283981" }, { "nct_id": "NCT04098146", "title": "Registry to Collect Data on Patients Undergoing Segmental Mandibular Defect Reconstruction Following Oral Squamous Cell Carcinoma Resection and Drugs-induced Osteonecrosis", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Mandibular Reconstruction", "Segmental Mandibular Defects" ], "interventions": [ { "name": "Surgical Resection and Reconstruction", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "AO Innovation Translation Center", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 300, "start_date": "2022-09-12", "completion_date": "2030-12-31", "has_results": false, "last_update_posted_date": "2025-09-04", "last_synced_at": "2026-05-22T05:17:57.856Z", "location_count": 5, "location_summary": "Jacksonville, Florida • Chicago, Illinois • New Hyde Park, New York + 2 more", "locations": [ { "city": "Jacksonville", "state": "Florida" }, { "city": "Chicago", "state": "Illinois" }, { "city": "New Hyde Park", "state": "New York" }, { "city": "New York", "state": "New York" }, { "city": "Fort Worth", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04098146" }, { "nct_id": "NCT07245758", "title": "Facial iD Customized Mandible Reconstruction Plates", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Mandibular Fractures", "Mandible Fracture", "Mandible; Deformity", "MANDIBLE", "Orthognathic Surgical Procedures" ], "interventions": [ { "name": "Mandibular reconstruction", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Stryker Craniomaxillofacial", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 50, "start_date": "2024-12-01", "completion_date": "2026-04-04", "has_results": false, "last_update_posted_date": "2026-04-22", "last_synced_at": "2026-05-22T05:17:57.856Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT07245758" }, { "nct_id": "NCT05754190", "title": "Assessing Symptom and Mood Dynamics in Pain Using the Smartphone Application SOMA", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Chronic Pain", "Acute Pain", "Post Operative Pain", "Fibromyalgia, Primary", "Fibromyalgia, Secondary", "Fibromyalgia", "Irritable Bowel Syndrome", "Chronic Headache Disorder", "Chronic Migraine", "Chronic Pelvic Pain Syndrome", "Temporomandibular Joint Disorders", "Endometriosis-related Pain", "Arthritis", "Chronic Low-back Pain", "Failed Back Surgery Syndrome", "Post Herpetic Neuralgia", "Neuropathic Pain", "Painful Diabetic Neuropathy", "Painful Bladder Syndrome", "Trauma-related Wound", "Trauma, Multiple", "Chronic Pain Syndrome", "Chronic Shoulder Pain" ], "interventions": [ { "name": "SOMA pain manager smartphone application", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Brown University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 800, "start_date": "2023-06-20", "completion_date": "2026-05-30", "has_results": false, "last_update_posted_date": "2025-09-19", "last_synced_at": "2026-05-22T05:17:57.856Z", "location_count": 1, "location_summary": "Providence, Rhode Island", "locations": [ { "city": "Providence", "state": "Rhode Island" } ], "official_url": "https://clinicaltrials.gov/study/NCT05754190" }, { "nct_id": "NCT00782171", "title": "Evaluation of Immediate Versus Delayed Loading of Dental Implants With a Modified Surface", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Partial Edentulism" ], "interventions": [ { "name": "SLActive dental implant", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Institut Straumann AG", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 266, "start_date": "2004-07", "completion_date": "2010-02", "has_results": true, "last_update_posted_date": "2017-06-20", "last_synced_at": "2026-05-22T05:17:57.856Z", "location_count": 3, "location_summary": "Boca Raton, Florida • Indianapolis, Indiana • Philadelphia, Pennsylvania", "locations": [ { "city": "Boca Raton", "state": "Florida" }, { "city": "Indianapolis", "state": "Indiana" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00782171" }, { "nct_id": "NCT05205616", "title": "Trial of Bilateral Sagittal Split Osteotomy Induced Paresthesia Using Ultrasonic vs. Reciprocating Saw Instrumentation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Surgical Complication", "Paresthesia", "Fracture", "Nerve Injury", "Nerve Entrapments", "Mandibular Nerve Injuries", "Mandibular Hypoplasia", "Mandibular Retrognathism", "Mandibular Hyperplasia", "Mandibular Prognathism" ], "interventions": [ { "name": "Sonopet ultrasonic saw", "type": "DEVICE" }, { "name": "Reciprocating saw", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": "45 Years", "sex": "ALL", "summary": "Up to 45 Years" }, "enrollment_count": 32, "start_date": "2021-07-20", "completion_date": "2023-07-25", "has_results": true, "last_update_posted_date": "2025-06-04", "last_synced_at": "2026-05-22T05:17:57.856Z", "location_count": 2, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05205616" }, { "nct_id": "NCT07245810", "title": "Stryker Facial iD Universal Plate Configurator: A Retrospective Post Market Follow Up", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Mandibular Fractures", "Facial Fracture", "Maxilla Fracture", "Orthognathic Surgical Procedures" ], "interventions": [ { "name": "Orthognatic surgery, Reconstructive maxillofacial surgery, Mandible and maxillofacial trauma surgery", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Stryker Craniomaxillofacial", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 726, "start_date": "2024-11-18", "completion_date": "2026-05-31", "has_results": false, "last_update_posted_date": "2026-04-22", "last_synced_at": "2026-05-22T05:17:57.856Z", "location_count": 2, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07245810" }, { "nct_id": "NCT06037161", "title": "Comparison of Two Methods of Covering a Single Lower Front Tooth With Receded Gums", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Recession, Gingival" ], "interventions": [ { "name": "Mandibular Incisor root coverage procedure", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Case Western Reserve University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 36, "start_date": "2023-05-19", "completion_date": "2027-07-30", "has_results": false, "last_update_posted_date": "2026-05-20", "last_synced_at": "2026-05-22T05:17:57.856Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT06037161" }, { "nct_id": "NCT03127943", "title": "Clinical Outcomes Mandible: Buffered 1% vs. Non-Buffered 1% Lidocaine", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Anesthesia, Local" ], "interventions": [ { "name": "Lidocaine", "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": "30 Years", "sex": "ALL", "summary": "18 Years to 30 Years" }, "enrollment_count": 24, "start_date": "2017-05-01", "completion_date": "2018-04-01", "has_results": true, "last_update_posted_date": "2019-02-06", "last_synced_at": "2026-05-22T05:17:57.856Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03127943" }, { "nct_id": "NCT00001600", "title": "Diagnosis and Evaluation of Patients Needing Third Molar (Wisdom Tooth) Extraction and Patients With Chronic Facial Pain", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Facial Pain", "Temporomandibular Joint Disorder" ], "interventions": [], "intervention_types": [], "sponsor": "National Institute of Dental and Craniofacial Research (NIDCR)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 4000, "start_date": "1997-08", "completion_date": "2005-08", "has_results": false, "last_update_posted_date": "2008-03-04", "last_synced_at": "2026-05-22T05:17:57.856Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT00001600" } ] }