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Myotonic Dystrophy 1

Clinical trial condition

Myotonic Dystrophy 1

Explore clinical trials studying Myotonic Dystrophy 1. Study availability and eligibility vary by location and protocol.

38 public trials 11 recruiting studies

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Myotonic Dystrophy 1 trial results

Completed

DM-IMT - Controlled, Randomized, Three-arm Intervention Study on the Safety and Efficacy of Regular Respiratory Muscle Training in Patients With Myotonic Dystrophy Type 1

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

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Completed

Effect of MYODM on Quality of Life, Fatigue and Hypersomnia in Patients With Myotonic Dystrophy Type 1

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

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Completed

Myotonic Dystrophy Type 1 Aerobic Exercise Study

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

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Completed

Effects of a 12-week Strength Training Program in Men With Myotonic Dystrophy Type 1

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

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Completed

Effects of a Multiple Component Training Program on Muscles in Adults With Myotonic Dystrophy Type 1

NCT04001920

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

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Completed

Study of Ranolazine in Myotonia Congenita, Paramyotonia Congenita and Myotonic Dystrophy Type 1

NCT02251457

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +12 more
Locations: The Ohio State University Wexner Medical Center Columbus, Ohio, United States

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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

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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