NCT04835298
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- Chu Reims Reims, France
Clinical trial condition
Myotonic Disorders
Explore clinical trials studying Myotonic Disorders. Study availability and eligibility vary by location and protocol.
117 public trials
41 recruiting studies
Myotonic Disorders trial results
NCT04052958
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- Friedrich-Baur-Institute, Dep. of Neurology Klinikum der Universitaet Muenchen Munich, Germany Munich, Bavaria, Germany
NCT04634682
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- Hospital Universitario Donostia San Sebastián, Guipuzkoa, Spain
NCT04187482
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- McMaster University Medical Center Hamilton, Ontario, Canada
NCT00577577
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- University of California Irvine Medical Center; MDA, ALS and Neuromuscular Center Orange, California, United States
- University of California, Davis Sacramento, California, United States
- University of Kansas Medical Center Kansas City, Kansas, United States
- Johns Hopkins Hospital Baltimore, Maryland, United States
NCT04018820
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- Groupe de recherche interdisciplinaire sur les maladies neuromusculaires Saguenay, Quebec, Canada
Completed
Safety, Tolerability and Pharmacokinetics of ERX-963 in Adults With Myotonic Dystrophy Type 1
NCT03959189
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disorders of Excessive Somnolence, Dyssomnias, +15 more
- Locations
-
- Stanford Neurosciences Health Center Palo Alto, California, United States
- Sleep Medicine Specialists of South Florida Miami, Florida, United States
- University of Iowa Iowa City, Iowa, United States
- The Center for Sleep & Wake Disorders Chevy Chase, Maryland, United States
NCT02831504
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- Newcastle-upon-Tyne Hospitals NHS Trust Newcastle upon Tyne, Tyne and Wear, United Kingdom
- University College London Hospitals NHS Foundation Trust, National Hospital for Neurology and Neurosurgery London, United Kingdom
NCT03603171
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
- Locations
-
- Friedrich-Baur-Institute, Dep. of Neurology Klinikum der Universitaet Muenchen Munich, Germany Munich, Bavaria, Germany
Completed
Sleep Breathing Disorders, a Main Trigger for Cardiac ARythmias in Type I Myotonic Dystrophy ?
NCT02375087
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
- Locations
-
- CHU Grenoble, France
Related conditions
- Heredodegenerative Disorders, Nervous System (117)
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities (116)
- Nervous System Diseases (116)
- Neurodegenerative Diseases (116)
- Genetic Diseases, Inborn (114)
- Musculoskeletal Diseases (114)
- Muscular Diseases (107)
- Muscular Disorders, Atrophic (104)