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Myotonic Dystrophy

Clinical trial condition

Myotonic Dystrophy

Explore clinical trials studying Myotonic Dystrophy. Study availability and eligibility vary by location and protocol.

107 public trials 36 recruiting studies

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Myotonic Dystrophy trial results

Completed

Multicenter Observational Study of Myotonic Dystrophy Type 1

NCT02308657

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +10 more
Locations: Stanford University Stanford, California, United States

University of Florida Gainesville, Florida, United States

University of Kansas Medical Center Kansas City, Kansas, United States

NIH Bethesda, Maryland, United States

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Completed

Observational Prolonged Trial in Myotonic Dystrophy Type 1

NCT02118779

Conditions: Behavior, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +12 more
Locations: Assistance Publique-Hospitaux de Paris Paris, France

Friedrich Naur Institute Munich, Germany

Radboud University Nijmegen Medical Centre Nijmegen, Netherlands

Newcastle University Newcastle, United Kingdom

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Completed

Venous Thromboembolism in DM1

NCT03141749

Conditions: Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Deep Vein Thrombosis, +23 more
Locations: Not specified

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Completed

Efficacy and Tolerance of AVAPS Mode in Myotonic Dystrophy

NCT01530841

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +13 more
Locations: Home ventilation Unit , Raymond Poincaré hospital Garches, Paris Area, France

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Completed

Lamotrigine as Treatment of Myotonia

NCT01939561

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dystrophia Myotonica Type 1, Genetic Diseases, Inborn, +26 more
Locations: Copenhagen Neuromuscular Center, department of Neurology, Rigshospitalet Copenhagen, Denmark

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Completed

Tracking the Brain in Myotonic Dystrophies: a 5-year Longitudinal Follow-up Study

NCT02729597

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +11 more
Locations: Not specified

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Completed

Study of Muscle Wasting and Altered Metabolism in Patients With Myotonic Dystrophy

NCT00004769

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +15 more
Locations: Not specified

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Completed

Effects of SomatoKine (Iplex)Recombinant Human Insulin-like Growth Factor-1/Recombinant Human Insulin-like Growth Factor-binding Protein-3 (rhIGF-I/rhIGFBP-3) in Myotonic Dystrophy Type 1 (DM1)

NCT00233519

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
Locations: University of Rochester Medical Center Rochester, New York, United States

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Completed

DM1 Heart Registry - DM1 Respiratory Registry

NCT01136330

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Death, Death, Sudden, +16 more
Locations: Pitié Salpêtrière Hospital Paris, Île-de-France Region, France

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Completed

Methylphenidate in Myotonic Dystrophy Type 1

NCT01421992

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disorders of Excessive Somnolence, Dyssomnias, +15 more
Locations: Institute of Readaptation in Physical Deficiency Québec, Quebec, Canada

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