NCT07502989
- Conditions
- Congenital Myopathy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Distal Myopathies, +16 more
- Locations
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- Beth Israel Deaconess Medical Center Boston, Massachusetts, United States
Clinical trial condition
Myotonia Congenita
Explore clinical trials studying Myotonia Congenita. Study availability and eligibility vary by location and protocol.
26 public trials
8 recruiting studies
Myotonia Congenita trial results
NCT00272883
- Conditions
- Central Core Disease, Centronuclear Myopathy, Congenital Fiber Type Disproportion, +19 more
- Locations
-
- Genetics Division, Boston Children's Hospital Boston, Massachusetts, United States
NCT07415837
- Conditions
- Congenital Myopathies, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne / Becker Muscular Dystrophy, +16 more
- Locations
-
- CHU de Clermont-Ferrand Clermont-Ferrand, France
NCT06287762
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
- Locations
-
- National Institutes of Health Clinical Center Bethesda, Maryland, United States
NCT07138963
- Conditions
- Congenital Muscular Dystrophies, Congenital Myopathies, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +14 more
- Locations
-
- Ain Shams University Cairo, Egypt
Recruiting
Transcriptomic Analysis to Put an End to Misdiagnosis in Patients With Rare Muscle Diseases
NCT06833489
- Conditions
- Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +27 more
- Locations
-
- Hopital Timone Marseille, France
NCT06157268
- Conditions
- Central Core Disease, Centronuclear Myopathy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +15 more
- Locations
-
- Radboudumc Nijmegen, Gelderland, Netherlands
- UMC Utrecht Utrecht, Netherlands
NCT01403402
- Conditions
- Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Fatty Liver and Infantile-onset Cataract Caused by TRAPPC11 Mutations), Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan and Epilepsy), Alpha-Dystroglycanopathy (Congenital Muscular Dystrophy With Hypoglycosylation of Dystroglycan), +89 more
- Locations
-
- Congenital Muscle Disease International Registry (www.cmdir.org) Lakewood, California, United States
Not Yet Recruiting
VirtualPark_Pediatric
NCT07580365
- Conditions
- Congenital Myopathies, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dystrophinopathy, +11 more
- Locations
-
- IRCCS E. Medea - La Nostra Famiglia Bosisio Parini, LC, Italy
- IRCCS Fondazione Stella Maris Pisa, PI, Italy
- IRCCS Fondazione Mondino Pavia, PV, Italy
- Fondazione Don Gnocchi - Centro "S. Maria al Mare" Salerno, SA, Italy
Not Yet Recruiting
The Prevalence of RYR1-related Disease
NCT06791369
- Conditions
- Body Temperature Changes, Central Core Disease, Centronuclear Myopathy, +26 more
- Locations
-
- King's College London London, United Kingdom