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Clinical trial condition

Muscular Dystrophy, Facioscapulohumeral

Explore clinical trials studying Muscular Dystrophy, Facioscapulohumeral. Study availability and eligibility vary by location and protocol.

67 public trials 18 recruiting studies
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Muscular Dystrophy, Facioscapulohumeral trial results

Completed

Safety, Tolerability, Pharmacokinetics, and Biological Activity of ATYR1940 in Adult Participants With Muscular Dystrophy

NCT02239224

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy (FSHD), Genetic Diseases, Inborn, +7 more
Locations
  • aTyr Pharma Investigative Site Rochester, New York, United States
  • aTyr Pharma Investigative Site Columbus, Ohio, United States
  • aTyr Pharma Investigative Site Marseille, France
  • aTyr Pharma Investigative Site Rome, Italy
View Trial Details
Completed

Evaluation of a Textile Scapula Orthosis

NCT04154098

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscle Weakness, +15 more
Locations
  • Kliniken Schmieder Konstanz Konstanz, Basen-Wuerttemberg, Germany
  • ETH Zurich Zurich, Switzerland
View Trial Details
Completed

Bone Health in Facioscapulohumeral Muscular Dystrophy

NCT02413190

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +7 more
Locations
  • Kennedy Krieger Institute, Johns Hopkins School of Medicine Baltimore, Maryland, United States
  • Concord Hospital Neurology Department, Hospital Road, Concord NSW 2139 Sydney, Australia
View Trial Details
Completed

Facioscapulohumeral Dystrophy in Children

NCT02625662

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +12 more
Locations
  • Radboud University Medical Center Nijmegen, Gelderland, Netherlands
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Completed

Acceptance and Commitment Therapy for Muscle Disease

NCT02810028

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, +12 more
Locations
  • King's College Hospital; The Royal London Hospital; University Hospital Southampton; King's College London London, United Kingdom
View Trial Details
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

A Multicenter Collaborative Study on the Clinical Features, Expression Profiling, and Quality of Life of Infantile Onset FSHD

NCT01437345

Conditions
Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +7 more
Locations
  • University of California - Davis Sacramento, California, United States
  • Children's National Medical Center Washington D.C., District of Columbia, United States
  • University of Minnesota Minneapolis, Minnesota, United States
  • Washington University St Louis, Missouri, United States
View Trial Details

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