NCT02032979
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +6 more
- Locations
-
- Hôpital Pasteur Nice, France
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
Muscular Dystrophy, Facioscapulohumeral trial results
NCT02579239
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +10 more
- Locations
-
- University of California, Irvine, ALS and Neuromuscular Center Irvine, California, United States
- Kennedy Krieger Institute; The Johns Hopkins University School of Medicine Baltimore, Maryland, United States
- OSU Wexner Medical Center Columbus, Ohio, United States
- Rigshospitalet, University of Copenhagen Copenhagen, Denmark
NCT02603562
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy (FSHD), Genetic Diseases, Inborn, +7 more
- Locations
-
- Stanford University Stanford, California, United States
- University of Iowa Children's Hospital Iowa City, Iowa, United States
- OSU Wexner Medical Center Columbus, Ohio, United States
- University of Utah Salt Lake City, Utah, United States
NCT05178706
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +7 more
- Locations
-
- Istanbul University-Cerrahpaşa Istanbul, Turkey (Türkiye)
NCT02531217
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +7 more
- Locations
-
- aTyr Pharma Investigative Site Columbus, Ohio, United States
- aTyr Pharma Investigative Site Rome, Italy
- aTyr Pharma Investigative Site Nijmegen, Netherlands
Completed
Study of Testosterone and rHGH in FSHD
NCT03123913
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, +7 more
- Locations
-
- University of Rochester Rochester, New York, United States
NCT02948244
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, FSHD1, FSHD2, +9 more
- Locations
-
- The Royal Children's Hospital Melbourne, Victoria, Australia
NCT05239520
- Conditions
- Arthralgia, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facio-Scapulo-Humeral Dystrophy, +17 more
- Locations
-
- Robert Jones & Agnes Hunt Orthopaedic Hospital Oswestry, Gobowen, United Kingdom
Completed
Examination of Operative Approach in pwFSHD (Patient With Facioscapulohumeral Muscular Dystrophy)
NCT05022355
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Facio-Scapulo-Humeral Dystrophy, Genetic Diseases, Inborn, +7 more
- Locations
-
- Istanbul University-Cerrahpaşa Istanbul, Turkey (Türkiye)
NCT04999735
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Muscular Diseases, +6 more
- Locations
-
- Centre for Human Drug Research Leiden, South Holland, Netherlands