{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Musculoskeletal+Injury+Trauma&page=3", "query": { "condition": "Musculoskeletal Injury Trauma", "page": 3 }, "page_size": 10 }, "pagination": { "page": 3, "page_size": 10, "total_count": 337, "total_pages": 34, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Musculoskeletal+Injury+Trauma&page=4&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Musculoskeletal+Injury+Trauma&page=2&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-01T00:00:14.684Z", "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": "NCT01393444", "title": "ECoG Direct Brain Interface for Individuals With Upper Limb Paralysis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Tetraplegia", "Spinal Cord Injury", "Brachial Plexus Injury", "Muscular Dystrophy", "ALS", "Brainstem Stroke" ], "interventions": [ { "name": "Implantation of ECoG sensors on the brain surface", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 6, "start_date": "2011-05", "completion_date": "2015-04", "has_results": true, "last_update_posted_date": "2016-12-12", "last_synced_at": "2026-10-01T00:00:14.684Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01393444" }, { "nct_id": "NCT01538459", "title": "Plasma Glucose Levels With Dexamethasone as Adjuvant to Interscalene Block", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Shoulder Pain", "Injury of Shoulder Region", "Disorder of Shoulder", "Disorder of Rotator Cuff", "Disorder of Tendon of Biceps" ], "interventions": [ { "name": "Dexamethasone", "type": "DRUG" }, { "name": "Bupivacaine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Lifespan", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 0, "start_date": "2012-11", "completion_date": "2013-11", "has_results": false, "last_update_posted_date": "2013-05-20", "last_synced_at": "2026-10-01T00:00:14.684Z", "location_count": 1, "location_summary": "Newport, Rhode Island", "locations": [ { "city": "Newport", "state": "Rhode Island" } ], "official_url": "https://clinicaltrials.gov/study/NCT01538459" }, { "nct_id": "NCT04393922", "title": "Spasticity After Spinal Cord Injury", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injuries" ], "interventions": [ { "name": "Acoustic stimuli (Startle)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Shirley Ryan AbilityLab", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 120, "start_date": "2020-05-13", "completion_date": "2024-05-18", "has_results": false, "last_update_posted_date": "2022-06-22", "last_synced_at": "2026-10-01T00:00:14.684Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT04393922" }, { "nct_id": "NCT06455969", "title": "Adaptions and Resiliency to Multi-Stressor OpeRations", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Musculoskeletal Injury", "Hypogonadism", "Hormonal Contraception" ], "interventions": [ { "name": "Goserelin 3.6 MG", "type": "DRUG" }, { "name": "Multi-Stressor Training", "type": "OTHER" }, { "name": "Testosterone gel (AndroGel 5g)", "type": "DRUG" }, { "name": "Testosterone gel (AndroGel 1.25g)", "type": "DRUG" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Bradley Nindl", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "ALL", "summary": "18 Years to 40 Years" }, "enrollment_count": 120, "start_date": "2024-07-15", "completion_date": "2027-08", "has_results": false, "last_update_posted_date": "2026-08-18", "last_synced_at": "2026-10-01T00:00:14.684Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06455969" }, { "nct_id": "NCT01307475", "title": "Study of Quality of Life in Freeman-Sheldon Syndrome and Related Conditions", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Arthrogryposis", "Craniofacial Abnormalities", "Posttraumatic Stress Disorder", "Depressive Disorder" ], "interventions": [ { "name": "PTSD Checklist-Specific", "type": "OTHER" }, { "name": "Modified Flanagan Quality of Life Scale", "type": "OTHER" }, { "name": "Center for Epidemiologic Studies Depression Scale", "type": "OTHER" }, { "name": "Functional Enquiry Form", "type": "OTHER" }, { "name": "Strength, Joint ROM, Girth and Length Measurements", "type": "OTHER" }, { "name": "Study Physical Examination", "type": "OTHER" }, { "name": "PTSD, Depression, and FSS-Focused Examination", "type": "OTHER" }, { "name": "Freeman-Sheldon Specific Quality of Life Survey", "type": "OTHER" }, { "name": "Lactate, Glucose, and Adenosine Triphosphate Blood Levels", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Freeman-Sheldon Research Group, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 6, "start_date": "2011-02", "completion_date": "2017-04-01", "has_results": false, "last_update_posted_date": "2017-04-04", "last_synced_at": "2026-10-01T00:00:14.684Z", "location_count": 1, "location_summary": "Buckhannon, West Virginia", "locations": [ { "city": "Buckhannon", "state": "West Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01307475" }, { "nct_id": "NCT03571737", "title": "Efficacy of Lidocaine Patch in Acute Musculoskeletal Pain in the Emergency Department", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Acute Musculoskeletal Disease", "Sprains", "Sprains and Strains", "Injuries", "Emergencies", "Trauma", "Acute Pain" ], "interventions": [ { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Lidocaine Patch 4%", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "East Carolina University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 23, "start_date": "2018-06-23", "completion_date": "2021-01-30", "has_results": true, "last_update_posted_date": "2024-03-25", "last_synced_at": "2026-10-01T00:00:14.684Z", "location_count": 1, "location_summary": "Greenville, North Carolina", "locations": [ { "city": "Greenville", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03571737" }, { "nct_id": "NCT00826228", "title": "Effect of Parathyroid Hormone (PTH) and Weight-Bearing on Bone in Spinal Cord Injury (SCI)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Osteoporosis", "Bone Loss", "Spinal Cord Injury" ], "interventions": [ { "name": "teriparatide", "type": "DRUG" }, { "name": "weight-bearing", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Thomas J. Schnitzer", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 12, "start_date": "2009-06", "completion_date": "2012-12", "has_results": true, "last_update_posted_date": "2013-07-11", "last_synced_at": "2026-10-01T00:00:14.684Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT00826228" }, { "nct_id": "NCT05456295", "title": "Comparative Effect of Carbon Fiber Orthosis Cuff Design on Preference, Comfort, and Mechanics", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Healthy", "Lower Limb Injury", "Post-Traumatic Osteoarthritis" ], "interventions": [ { "name": "Carbon Fiber Custom Dynamic Orthosis (CDO)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Iowa", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 35, "start_date": "2023-05-17", "completion_date": "2025-09-29", "has_results": false, "last_update_posted_date": "2026-01-15", "last_synced_at": "2026-10-01T00:00:14.684Z", "location_count": 1, "location_summary": "Iowa City, Iowa", "locations": [ { "city": "Iowa City", "state": "Iowa" } ], "official_url": "https://clinicaltrials.gov/study/NCT05456295" }, { "nct_id": "NCT02195895", "title": "Effect of Alendronate on Bone in People With Chronic Spinal Cord Injury (SCI) Previously Treated With Teriparatide", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Spinal Cord Injury", "Bone Loss", "Osteoporosis" ], "interventions": [ { "name": "Alendronate", "type": "DRUG" }, { "name": "Calcium", "type": "DIETARY_SUPPLEMENT" }, { "name": "Vitamin D", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DRUG", "DIETARY_SUPPLEMENT" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 17, "start_date": "2014-04", "completion_date": "2016-08-05", "has_results": true, "last_update_posted_date": "2023-03-30", "last_synced_at": "2026-10-01T00:00:14.684Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT02195895" }, { "nct_id": "NCT01347892", "title": "DeNovo NT Ankle LDC Study", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Defect of Articular Cartilage", "Osteochondral Lesion of Talus", "Osteochondritis Dissecans" ], "interventions": [ { "name": "DeNovo NT Natural Tissue Graft", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Zimmer Orthobiologics, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 205, "start_date": "2011-03", "completion_date": "2019-09", "has_results": false, "last_update_posted_date": "2017-01-26", "last_synced_at": "2026-10-01T00:00:14.684Z", "location_count": 8, "location_summary": "Sacramento, California • Honolulu, Hawaii • Baltimore, Maryland + 5 more", "locations": [ { "city": "Sacramento", "state": "California" }, { "city": "Honolulu", "state": "Hawaii" }, { "city": "Baltimore", "state": "Maryland" }, { "city": "Edina", "state": "Minnesota" }, { "city": "Westerville", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01347892" } ] }