CompletedNCT01990976
Study of Morphology and Functional Magnetic Resonance Imaging (MRI) Muscle Patients With Muscular Dystrophy Type FSHD Benefiting a Physical Training Introduced.
Studying Congenital muscular dystrophy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Centre Hospitalier Universitaire de Saint Etienne
- Principal Investigator
- Léonard FEASSON, MD-PhDCHU de Saint-Etienne
- Intervention
- MRI(device)
- Enrollment
- 15 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2012 – 2015
Study locations (2)
- CHU de Grenbole, Grenoble, France
- CHU de Saint-Etienne, Saint-Etienne, France
Collaborators
Association Française contre les Myopathies (AFM), Paris · Ministry of Health, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT01990976 on ClinicalTrials.govOther trials for Congenital muscular dystrophy
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