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Paramyotonia Congenita

Clinical trial condition

Paramyotonia Congenita

Explore clinical trials studying Paramyotonia Congenita. Study availability and eligibility vary by location and protocol.

4 public trials 0 recruiting studies

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Paramyotonia Congenita trial results

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

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

Mexiletine and Non Dystrophic Myotonias

NCT02336477

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Heredodegenerative Disorders, Nervous System, +9 more
Locations: Groupe Hospitalier Pitié Salpetriere Paris, France

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Completed

Phase III Randomized, Double-Blind, Placebo-Controlled Study of Dichlorphenamide for Periodic Paralyses and Associated Sodium Channel Disorders

NCT00004802

Conditions: Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Genetic Diseases, Inborn, +19 more
Locations: Not specified

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