{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Muscle+Disorders&page=21", "query": { "condition": "Muscle Disorders", "page": 21 }, "page_size": 10 }, "pagination": { "page": 21, "page_size": 10, "total_count": 3708, "total_pages": 371, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Muscle+Disorders&page=22&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Muscle+Disorders&page=20&page_size=10" }, "source": "remote", "last_synced_at": "2026-11-01T15:48:36.839Z", "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": "NCT04099667", "title": "Efficacy and Safety Study of MYOBLOC® in the Treatment of Adult Lower Limb Spasticity", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Spasticity" ], "interventions": [ { "name": "Phase 2; Low Dose MYOBLOC (15,000 Units)", "type": "DRUG" }, { "name": "Phase 2; High Dose MYOBLOC (20,000 Units)", "type": "DRUG" }, { "name": "Phase 2; Placebo", "type": "DRUG" }, { "name": "Phase 3; MYOBLOC", "type": "DRUG" }, { "name": "Phase 3; Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Solstice Neurosciences, LLC, a subsidiary of MDD US Operations, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 40, "start_date": "2019-12-17", "completion_date": "2023-03-24", "has_results": true, "last_update_posted_date": "2026-05-22", "last_synced_at": "2026-11-01T15:48:36.839Z", "location_count": 4, "location_summary": "Downey, California • Boise, Idaho • Port Royal, South Carolina + 1 more", "locations": [ { "city": "Downey", "state": "California" }, { "city": "Boise", "state": "Idaho" }, { "city": "Port Royal", "state": "South Carolina" }, { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04099667" }, { "nct_id": "NCT01226667", "title": "Fixed Versus Flexible Dosing of Pregabalin in Patients With Fibromyalgia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Fibromyalgia" ], "interventions": [ { "name": "Pregabalin", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Osteoporosis Medical Center, Beverly Hills, CA", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "18 Years to 65 Years · Female only" }, "enrollment_count": 174, "start_date": "2010-07", "completion_date": "2012-07", "has_results": false, "last_update_posted_date": "2012-07-31", "last_synced_at": "2026-11-01T15:48:36.839Z", "location_count": 5, "location_summary": "Beverly Hills, California • Huntington Beach, California • Tucson, California + 1 more", "locations": [ { "city": "Beverly Hills", "state": "California" }, { "city": "Beverly Hills", "state": "California" }, { "city": "Huntington Beach", "state": "California" }, { "city": "Tucson", "state": "California" }, { "city": "West Hills", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01226667" }, { "nct_id": "NCT00424892", "title": "Study Evaluating DVS SR in Patients With Fibromyalgia Syndrome", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Fibromyalgia" ], "interventions": [ { "name": "Desvenlafaxine Sustained Release", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Wyeth is now a wholly owned subsidiary of Pfizer", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 600, "start_date": null, "completion_date": "2007-06", "has_results": false, "last_update_posted_date": "2007-12-06", "last_synced_at": "2026-11-01T15:48:36.839Z", "location_count": 59, "location_summary": "Huntsville, Alabama • Mobile, Alabama • Phoenix, Arizona + 52 more", "locations": [ { "city": "Huntsville", "state": "Alabama" }, { "city": "Mobile", "state": "Alabama" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Anaheim", "state": "California" }, { "city": "Sacramento", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00424892" }, { "nct_id": "NCT01118988", "title": "Peer Mentorship: An Intervention To Promote Effective Pain Self-Management In Adolescents", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Irritable Bowel Syndrome (IBS)", "Functional Abdominal Pain", "Fibromyalgia", "Complex Regional Pain Syndrome (CRPS)", "Myofacial Pain", "Chronic Daily Headaches", "Migraine Headaches", "Chronic Pain" ], "interventions": [ { "name": "Mentorship", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "12 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "12 Years to 18 Years" }, "enrollment_count": 27, "start_date": "2009-12", "completion_date": "2011-06", "has_results": true, "last_update_posted_date": "2016-09-30", "last_synced_at": "2026-11-01T15:48:36.839Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01118988" }, { "nct_id": "NCT06100822", "title": "Managing Chronic Tendon Pain by Metformin", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Tendinopathy", "Chronic Pain", "Achilles Tendinopathy" ], "interventions": [ { "name": "Metformin", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "James Wang", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "18 Years to 50 Years" }, "enrollment_count": 21, "start_date": "2024-05-24", "completion_date": "2026-08-24", "has_results": false, "last_update_posted_date": "2026-08-27", "last_synced_at": "2026-11-01T15:48:36.839Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06100822" }, { "nct_id": "NCT00153179", "title": "Free Fatty Acids and Vascular Function in Subjects With Diabetes", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Type 2 Diabetes Mellitus" ], "interventions": [ { "name": "acipimox", "type": "DRUG" }, { "name": "placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Brigham and Women's Hospital", "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": 40, "start_date": "2005-09", "completion_date": "2013-03", "has_results": true, "last_update_posted_date": "2018-09-25", "last_synced_at": "2026-11-01T15:48:36.839Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00153179" }, { "nct_id": "NCT02838394", "title": "Dry Needling and Functional Improvement", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Myofascial Trigger Point Pain", "Myofascial Pain Syndrome" ], "interventions": [ { "name": "Dry needling", "type": "PROCEDURE" }, { "name": "Sham dry needling", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "Brigham Young 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": 20, "start_date": "2016-12", "completion_date": "2023-08", "has_results": false, "last_update_posted_date": "2024-04-25", "last_synced_at": "2026-11-01T15:48:36.839Z", "location_count": 1, "location_summary": "Provo, Utah", "locations": [ { "city": "Provo", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT02838394" }, { "nct_id": "NCT04626453", "title": "Oxygenation Changes After 2-month Exercise in Sedentary Older Adults With Diabetes", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetes Mellitus, Type 2", "Oxygen Deficiency" ], "interventions": [ { "name": "2-month home moderate-intensity exercise", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "State University of New York at Buffalo", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "60 Years", "maximum_age": null, "sex": "ALL", "summary": "60 Years and older" }, "enrollment_count": 81, "start_date": "2020-10-29", "completion_date": "2021-06-27", "has_results": false, "last_update_posted_date": "2021-09-21", "last_synced_at": "2026-11-01T15:48:36.839Z", "location_count": 1, "location_summary": "Buffalo, New York", "locations": [ { "city": "Buffalo", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04626453" }, { "nct_id": "NCT07329088", "title": "Isoleucine Addition Treatment Effects in a Controlled Diet Study", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prediabetes (Insulin Resistance, Impaired Glucose Tolerance)", "Metabolic Syndrome (MetS)", "Obesity & Overweight" ], "interventions": [ { "name": "L-Isoleucine", "type": "DIETARY_SUPPLEMENT" }, { "name": "Low-isoleucine diet", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "Jean L. Fry", "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": 0, "start_date": "2026-05-04", "completion_date": "2029-01-31", "has_results": false, "last_update_posted_date": "2026-04-15", "last_synced_at": "2026-11-01T15:48:36.839Z", "location_count": 1, "location_summary": "Lexington, Kentucky", "locations": [ { "city": "Lexington", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT07329088" }, { "nct_id": "NCT02854683", "title": "Reducing Orthostatic Intolerance With Oral Rehydration in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Chronic Fatigue Syndrome", "Myalgic Encephalomyelitis", "Systemic Exertion Intolerance Disease (SEID)", "Postural Tachycardia Syndrome (POTS)", "Neurally Mediated Syncope (NMS)" ], "interventions": [ { "name": "Normal Saline", "type": "DRUG" }, { "name": "Oral Rehydration Solution", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DRUG", "DIETARY_SUPPLEMENT" ], "sponsor": "New York Medical College", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "15 Years", "maximum_age": "29 Years", "sex": "ALL", "summary": "15 Years to 29 Years" }, "enrollment_count": 45, "start_date": "2016-02", "completion_date": "2021-12", "has_results": false, "last_update_posted_date": "2021-06-10", "last_synced_at": "2026-11-01T15:48:36.839Z", "location_count": 1, "location_summary": "Hawthorne, New York", "locations": [ { "city": "Hawthorne", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02854683" } ] }