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Glycogen Storage Disease Type 2 clinical trials

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NCT ID: NCT02708784 Enrolling by invitation - Clinical trials for Glycogen Storage Disease Type 2

An MRI Study on Muscular Diseases -Pompe Disease and Dystrophia Myotonica-

Start date: September 2015
Phase: N/A
Study type: Observational

The aim of the project is to develop new Magnetic Resonance (MR) imaging techniques for better diagnosis and monitoring of patients with muscular disorders. Muscle quality in patients with Late Onset Pompe Disease (Acid Maltase Deficiency type 2) and in patients with Myotonica Dystrophy will be evaluated, by determining muscle strength in relation to muscle size and muscle strength in relations to fat-muscle ratio.