Skip to main content

Find Clinical Trials

Home
Conditions
Muscular Dystrophies

Clinical trial condition

Muscular Dystrophies

Explore clinical trials studying Muscular Dystrophies. Study availability and eligibility vary by location and protocol.

165 public trials 36 recruiting studies

Refine in advanced search Browse all conditions

Muscular Dystrophies trial results

Completed

Rasch-analysis of Clinical Severity in FSHD

NCT02766985

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +7 more
Locations: University of Kansas Medical Center Kansas City, Kansas, United States

University of Utah Salt Lake City, Utah, United States

View Trial Details

Completed

Enhance Wellness for Individuals With Long-Term Physical Disabilities

NCT02815878

Conditions: Autoimmune Diseases, Autoimmune Diseases of the Nervous System, Central Nervous System Diseases, +30 more
Locations: University of Washington Seattle, Washington, United States

View Trial Details

Completed

Effect of EPA and DHA in the Inflammation and Metabolic Disorders in DMD/DMB Patients

NCT01826422

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: Unit of Medical Researcha in Nutrition, Pediatric Hospital, IMSS. Mexico City, Mexico

View Trial Details

Completed

Arrhythmias in Myotonic Muscular Dystrophy

NCT00622453

Conditions: Arrhythmia, Arrhythmias, Cardiac, Cardiovascular Diseases, +17 more
Locations: Krannert Institute of Cardiology Indianapolis, Indiana, United States

View Trial Details

Completed

Assessment of Response to Treatment of Osteoporosis With Oral Bisphosphonates in Patients With Muscular Dystrophy

NCT01882400

Conditions: Bone Diseases, Bone Diseases, Metabolic, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +17 more
Locations: Centre hospitalier universitaire de Sherbrooke Sherbrooke, Quebec, Canada

View Trial Details

Completed

Clinical Intramuscular Gene Transfer Trial of rAAVrh74.MCK.Micro-Dystrophin to Patients With Duchenne Muscular Dystrophy

NCT02376816

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne Muscular Dystrophy, Genetic Diseases, Inborn, +8 more
Locations: Nationwide Children's Hospital Columbus, Ohio, United States

View Trial Details

Completed

Safety and Efficacy of a Flavonoids- and omega3s-based Compound for the Treatment of Muscular Dystrophies

NCT03317171

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscle Inflammation, +8 more
Locations: Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico Milan, Italy

View Trial Details

Completed

A Clinical Study to Assess Two Doses of GSK2402968 in Subjects With Duchenne Muscular Dystrophy (DMD)

NCT01462292

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: GSK Investigational Site Sacramento, California, United States

GSK Investigational Site Stanford, California, United States

GSK Investigational Site Gulf Breeze, Florida, United States

GSK Investigational Site Iowa City, Iowa, United States

View all 14 locations

View Trial Details

Completed

GDF-15 as a Biomarker for Mitochondrial Disease

NCT02745938

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Metabolic Diseases, +11 more
Locations: Rigshospitalet Copenhagen, Copenhagen East., Denmark

View Trial Details

Completed

A Double-blind, Escalating Dose, Randomized, Placebo-controlled Study Assessing PK, Safety, Tolerability in Non-ambulant DMD Subjects

NCT01128855

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +7 more
Locations: GSK Investigational Site Columbus, Ohio, United States

GSK Investigational Site Paris, France

View Trial Details