{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Muscle+Recovery&page=5", "query": { "condition": "Muscle Recovery", "page": 5 }, "page_size": 10 }, "pagination": { "page": 5, "page_size": 10, "total_count": 110, "total_pages": 11, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Muscle+Recovery&page=6&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Muscle+Recovery&page=4&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-20T14:32:47.697Z", "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": "NCT05094362", "title": "Operant Conditioning of Spinal Reflexes Training System--Reflex Operant Down Conditioning", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injuries", "Neurological Injury", "Paralysis", "Spasticity, Muscle" ], "interventions": [ { "name": "Spinal Reflex Operant Down Conditioning", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Medical University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 25, "start_date": "2023-08-23", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-09-15", "last_synced_at": "2026-10-20T14:32:47.697Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05094362" }, { "nct_id": "NCT04230824", "title": "Chronic Study on Body Composition, Training, Performance, and Recovery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Damage Muscle", "Body Weight Changes", "Performance Enhancing Product Use" ], "interventions": [ { "name": "Pre-workout plus and Protein recovery plus", "type": "DIETARY_SUPPLEMENT" }, { "name": "Placebo", "type": "OTHER" }, { "name": "6-week resistance training program", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "Pharmanex", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "25 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "25 Years to 50 Years" }, "enrollment_count": 69, "start_date": "2021-02-01", "completion_date": "2022-01-01", "has_results": false, "last_update_posted_date": "2022-01-13", "last_synced_at": "2026-10-20T14:32:47.697Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04230824" }, { "nct_id": "NCT02909439", "title": "Quality of Recovery After Reversal With Neostigmine or Sugammadex.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Incomplete Reversal of Neuromuscular Block" ], "interventions": [ { "name": "Sugammadex", "type": "DRUG" }, { "name": "Neostigmine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Stony Brook University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 80, "start_date": "2016-11", "completion_date": "2018-02", "has_results": true, "last_update_posted_date": "2020-05-22", "last_synced_at": "2026-10-20T14:32:47.697Z", "location_count": 1, "location_summary": "Stony Brook, New York", "locations": [ { "city": "Stony Brook", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02909439" }, { "nct_id": "NCT06795425", "title": "A Randomized, Double-Blind Study to Assess the Effect of a Postbiotic on Oxidative Stress and Exercise Performance", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Oxidative Stress", "Healthy", "Exercise-induced Muscle Damage", "Exercise-induced Muscle Soreness", "Immune Function", "Gut Health", "Microbiome Analysis", "Exercise Performance", "Exercise Metabolism" ], "interventions": [ { "name": "Postbiotic Active Lifestyle Blend", "type": "DIETARY_SUPPLEMENT" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "Lindenwood University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "18 Years to 45 Years" }, "enrollment_count": 80, "start_date": "2025-02-01", "completion_date": "2026-01-01", "has_results": false, "last_update_posted_date": "2025-01-28", "last_synced_at": "2026-10-20T14:32:47.697Z", "location_count": 1, "location_summary": "Saint Charles, Missouri", "locations": [ { "city": "Saint Charles", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT06795425" }, { "nct_id": "NCT04314596", "title": "The Effects of Antioxidant Supplementation on Multiple Endurance Race Performance, Physiology, and Recovery.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Oxidative Stress", "Muscle Strength", "Resistance Training", "Body Composition", "Muscle Damage" ], "interventions": [ { "name": "Cross Training Course", "type": "OTHER" }, { "name": "Oceanix", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "OTHER", "DIETARY_SUPPLEMENT" ], "sponsor": "Applied Science & Performance Institute", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "18 Years to 45 Years" }, "enrollment_count": 18, "start_date": "2020-01-20", "completion_date": "2020-02-19", "has_results": false, "last_update_posted_date": "2020-03-19", "last_synced_at": "2026-10-20T14:32:47.697Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04314596" }, { "nct_id": "NCT07498166", "title": "Project Tendura: The Impact of Blood Flow Restriction Resistance Training (BFR-RT) in Patients With Achilles Tendon Rupture (ATR) Repair", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Achilles Tendon Rupture", "Blood Flow Restriction Therapy", "Achilles Tendon Repairs/Reconstructions", "Dynamic Blood Flow Restriction" ], "interventions": [ { "name": "Blood Flow Restriction Resistance Training (BFR-RT)", "type": "DEVICE" }, { "name": "Sham Blood Flow Restriction", "type": "DEVICE" }, { "name": "Standard Physical Therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "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": 75, "start_date": "2026-02-01", "completion_date": "2027-02-01", "has_results": false, "last_update_posted_date": "2026-04-01", "last_synced_at": "2026-10-20T14:32:47.697Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07498166" }, { "nct_id": "NCT02558946", "title": "Physical Therapy for Men Undergoing Prostatectomy", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prostate Cancer", "Urinary Incontinence", "Pelvic Floor Physical Therapy" ], "interventions": [ { "name": "Pelvic Floor Muscle Physical Therapy", "type": "BEHAVIORAL" }, { "name": "Control Group", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 113, "start_date": "2015-06-29", "completion_date": "2025-01", "has_results": false, "last_update_posted_date": "2024-11-04", "last_synced_at": "2026-10-20T14:32:47.697Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT02558946" }, { "nct_id": "NCT06723119", "title": "Effect of Resveratrol Supplementation on Exercise Performance and Recovery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Effect of Resveratrol on Performance and Recovery" ], "interventions": [ { "name": "Resveratrol (VRES) 500 mg oral once daily.", "type": "OTHER" }, { "name": "Placebo 500 mg oral once daily.", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Central Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "MALE", "summary": "18 Years to 40 Years · Male only" }, "enrollment_count": 20, "start_date": "2024-10-01", "completion_date": "2025-04-01", "has_results": false, "last_update_posted_date": "2024-12-09", "last_synced_at": "2026-10-20T14:32:47.697Z", "location_count": 1, "location_summary": "Orlando, Florida", "locations": [ { "city": "Orlando", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06723119" }, { "nct_id": "NCT06465407", "title": "Collagen Protein Versus Placebo on Muscle Recovery", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anthropometrics: Height and Weight", "Isometric Standing and Seated Plantarflexion", "Calf Muscle Thickness", "Achilles Tendon Length and Thickness", "Myotonography of the Calf Musculature and Achilles Tendon", "Pain Pressure Threshold of the Calf", "Pain Scale", "Endurance Calf Test", "Dietary Analysis" ], "interventions": [ { "name": "Collagen", "type": "DIETARY_SUPPLEMENT" }, { "name": "Maltodextrin", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "University of Central Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "30 Years", "sex": "MALE", "summary": "18 Years to 30 Years · Male only" }, "enrollment_count": 36, "start_date": "2024-07-01", "completion_date": "2024-12-01", "has_results": false, "last_update_posted_date": "2024-06-18", "last_synced_at": "2026-10-20T14:32:47.697Z", "location_count": 1, "location_summary": "Orlando, Florida", "locations": [ { "city": "Orlando", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06465407" }, { "nct_id": "NCT06030531", "title": "Spasticity and Functional Recovery After SCI", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Acute Spinal Cord Injury", "Spinal Cord Injuries" ], "interventions": [ { "name": "Measures of spasticity, connectivity and analysis of single nucleotide polymorphisms and biomarkers of inflammation", "type": "OTHER" }, { "name": "Analysis of biomarkers", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Shirley Ryan AbilityLab", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 240, "start_date": "2020-07-01", "completion_date": "2024-12-31", "has_results": false, "last_update_posted_date": "2023-09-11", "last_synced_at": "2026-10-20T14:32:47.697Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06030531" } ] }