{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Post+Traumatic+Deformity&page=2", "query": { "condition": "Post Traumatic Deformity", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Post+Traumatic+Deformity&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-07-24T07:09:19.071Z", "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": "NCT02175576", "title": "Randomized Controlled Clinical Outcomes of the Vanguard XP Bicruciate Knee System", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Osteoarthritis", "Rheumatoid Arthritis", "Traumatic Arthritis", "Lower Limb Deformity", "Post-traumatic Deformity", "Complications, Arthroplasty" ], "interventions": [ { "name": "Vanguard XP Bicruciate Knee System", "type": "DEVICE" }, { "name": "Vanguard CR Knee System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Zimmer Biomet", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 50, "start_date": "2014-10", "completion_date": "2020-12", "has_results": true, "last_update_posted_date": "2023-02-21", "last_synced_at": "2026-07-24T07:09:19.071Z", "location_count": 2, "location_summary": "Chicago, Illinois • Salt Lake City, Utah", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT02175576" }, { "nct_id": "NCT01542580", "title": "A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Osteoarthritis", "Rheumatoid Arthritis", "Traumatic Arthritis", "Post Traumatic Deformity", "Complications; Arthroplasty", "Deformity of Limb" ], "interventions": [ { "name": "Vanguard SSK 360 with PS Bearing", "type": "DEVICE" }, { "name": "Vanguard SSK 360 with PSC bearing", "type": "DEVICE" }, { "name": "Vanguard DA 360", "type": "DEVICE" }, { "name": "Vanguard 360 TiNbN Femur with PS bearing", "type": "DEVICE" }, { "name": "Vanguard 360 TiNbN Femur with PSC bearing", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Zimmer Biomet", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 255, "start_date": "2012-03", "completion_date": "2031-12", "has_results": false, "last_update_posted_date": "2025-11-25", "last_synced_at": "2026-07-24T07:09:19.071Z", "location_count": 4, "location_summary": "Morton Grove, Illinois • Henderson, Nevada • Salt Lake City, Utah + 1 more", "locations": [ { "city": "Morton Grove", "state": "Illinois" }, { "city": "Henderson", "state": "Nevada" }, { "city": "Salt Lake City", "state": "Utah" }, { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01542580" }, { "nct_id": "NCT04806620", "title": "Unhide® Project: A Digital Health Platform to Collect Lifestyle Data for Brain Inflammation Research", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Post-Acute COVID-19 Syndrome", "ME/CFS", "Rheumatic Arthritis", "Juvenile Rheumatoid Arthritis (JRA)", "Psoriatic Arthritis (PsA)", "Ankylosing Spondylitis (AS)", "Autoimmune Encephalitis", "Celiac Disease", "Celiac Disease in Children", "Chronic Lyme Disease", "Post-treatment Lyme Disease Syndrome", "Crohn's Disease", "Dysautonomia", "Anorexia Nervosa", "Bulimia Nervosa", "ARFID", "Avoidant / Restrictive Food Intake Disorder", "Ehlers Danlos Syndrome", "Endometriosis", "Fibromyalgia (FM)", "Long COVID", "Lupus", "Migraines", "Mast Cell Activation Syndrome", "Multiple Sclerosis", "Myalgic Encephalomyelitis (ME)", "Myasthenia Gravis, Generalized", "Myasthenia Gravis in Children", "Narcolepsy", "Obsessive Compulsive Disorder (OCD)", "PANDAS", "Pediatric Acute-onset Neuropsychiatric Syndrome (PANS)", "POTS - Postural Orthostatic Tachycardia Syndrome", "General Anxiety Disorder, Social Anxiety Disorder", "PTSD - Post Traumatic Stress Disorder", "Psoriasis", "Traumatic Brain Injury", "Tourette's Syndrome", "Inflammatory Bowel Disease (IBD)", "Autoimmune Diseases", "Neurological Diseases or Conditions", "Psychiatric Disorder", "Sjogren's Syndrome", "Ulcerative Colitis and Crohn's Disease" ], "interventions": [], "intervention_types": [], "sponsor": "Brain Inflammation Collaborative", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "2 Years", "maximum_age": null, "sex": "ALL", "summary": "2 Years and older" }, "enrollment_count": 10000, "start_date": "2023-07-05", "completion_date": "2030-12-31", "has_results": false, "last_update_posted_date": "2026-01-22", "last_synced_at": "2026-07-24T07:09:19.071Z", "location_count": 1, "location_summary": "Delafield, Wisconsin", "locations": [ { "city": "Delafield", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT04806620" }, { "nct_id": "NCT04785482", "title": "The PaTHS Descriptive Correlational Longitudinal Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Single-ventricle", "Posttraumatic Stress Disorder", "Psychosocial Impairment" ], "interventions": [], "intervention_types": [], "sponsor": "Children's Mercy Hospital Kansas City", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 22, "start_date": "2021-03-01", "completion_date": "2022-06-09", "has_results": false, "last_update_posted_date": "2022-07-22", "last_synced_at": "2026-07-24T07:09:19.071Z", "location_count": 1, "location_summary": "Kansas City, Missouri", "locations": [ { "city": "Kansas City", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT04785482" }, { "nct_id": "NCT05037734", "title": "A Randomized Controlled Trial for Partial Knee Arthroplasty", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Degenerative Joint Disease of Knee", "Osteoarthritis", "Traumatic Arthritis", "Varus Deformity", "Knee Pain Chronic" ], "interventions": [ { "name": "Persona Partial Knee System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Zimmer Biomet", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 0, "start_date": "2023-06", "completion_date": "2030-12", "has_results": false, "last_update_posted_date": "2023-06-05", "last_synced_at": "2026-07-24T07:09:19.071Z", "location_count": 1, "location_summary": "Jackson, Mississippi", "locations": [ { "city": "Jackson", "state": "Mississippi" } ], "official_url": "https://clinicaltrials.gov/study/NCT05037734" }, { "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": "2026-07-24T07:09:19.071Z", "location_count": 1, "location_summary": "Buckhannon, West Virginia", "locations": [ { "city": "Buckhannon", "state": "West Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01307475" }, { "nct_id": "NCT03756506", "title": "The Use of a Novel Microbicidal Liquid Polymer for the Reduction of Pin Track Infection", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Infection", "Post-operative Care" ], "interventions": [ { "name": "Novel Microbicidal Liquid Polymer", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Prevent-Plus LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 13, "start_date": "2018-11-07", "completion_date": "2019-09-30", "has_results": true, "last_update_posted_date": "2021-03-30", "last_synced_at": "2026-07-24T07:09:19.071Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT03756506" }, { "nct_id": "NCT04968405", "title": "Catalyst CSR Shoulder System for Semi or Total Shoulder Arthroplasty", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Osteoarthritis Shoulder", "Avascular Necrosis of the Head of Humerus", "Rheumatoid Arthritis Shoulder" ], "interventions": [ { "name": "Catalyst CSR Total Shoulder System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Catalyst OrthoScience", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 87, "start_date": "2022-07-22", "completion_date": "2026-02-01", "has_results": false, "last_update_posted_date": "2026-03-31", "last_synced_at": "2026-07-24T07:09:19.071Z", "location_count": 3, "location_summary": "Royal Oak, Michigan • Portland, Oregon • Providence, Rhode Island", "locations": [ { "city": "Royal Oak", "state": "Michigan" }, { "city": "Portland", "state": "Oregon" }, { "city": "Providence", "state": "Rhode Island" } ], "official_url": "https://clinicaltrials.gov/study/NCT04968405" }, { "nct_id": "NCT03048201", "title": "Physica System Total Knee Replacement Registry Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Osteoarthritis, Knee", "Traumatic Arthritis", "Avascular Necrosis", "Degenerative Joint Disease of Knee", "Rheumatoid Arthritis", "Deformity of Knee" ], "interventions": [ { "name": "Physica Kinematic Retaining Knee System", "type": "DEVICE" }, { "name": "Physica Cruciate Retaining Knee System", "type": "DEVICE" }, { "name": "Physica Posterior Stabilized Knee System", "type": "DEVICE" }, { "name": "Physica Cruciate Retaining Knee System with LMC Liner", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Limacorporate S.p.a", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": null, "sex": "ALL", "summary": "22 Years and older" }, "enrollment_count": 800, "start_date": "2017-03-24", "completion_date": "2030-03", "has_results": false, "last_update_posted_date": "2023-03-21", "last_synced_at": "2026-07-24T07:09:19.071Z", "location_count": 5, "location_summary": "Rancho Mirage, California • Daytona Beach, Florida • Aurora, Illinois + 2 more", "locations": [ { "city": "Rancho Mirage", "state": "California" }, { "city": "Daytona Beach", "state": "Florida" }, { "city": "Aurora", "state": "Illinois" }, { "city": "Syracuse", "state": "New York" }, { "city": "Oklahoma City", "state": "Oklahoma" } ], "official_url": "https://clinicaltrials.gov/study/NCT03048201" }, { "nct_id": "NCT01075672", "title": "Outcomes of Cognitive Behavioral Therapy (CBT) Interventions Provided by Unlicensed Professionals", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obsessive Compulsive Disorder", "Body Dysmorphic Disorder", "Tourette Syndrome", "Trichotillomania", "Panic Disorder", "Social Phobia", "Generalized Anxiety Disorder", "Depression", "Post-Traumatic Stress Disorder", "Attention Deficit Hyperactivity Disorder", "Eating Disorder", "Specific Phobia", "General Medical Condition" ], "interventions": [ { "name": "Cognitive behavioral therapy (CBT)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 250, "start_date": "2010-01", "completion_date": "2027-01", "has_results": false, "last_update_posted_date": "2026-02-23", "last_synced_at": "2026-07-24T07:09:19.071Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01075672" } ] }