Walking ANalysis Interest in Persons wiTh facioscapulohumEral Muscular Dystrophies

Recruiting N/A Interventional Study
Facioscapulohumeral Dystrophy
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
60 (estimated)
Sponsor
Centre Hospitalier Universitaire Dijon · Other
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About This Trial
Facioscapulohumeral muscular dystrophy (FSH) is one of the most common genetic myopathies in adults. It is characterised by progressive asymmetric muscular atrophy affecting the skeletal muscles of the face, upper limbs and then lower limbs, causing problems with walking, which is one of the most frequent complaints of these patients. In fact, 20% of people with FSH require a wheelchair from the a…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: Patient : * Adult ; * Having given written consent; * With an established molecular genetic diagnosis of FSH; * Able to understand the instructions for carrying out the various tests; * Able to walk for at least 6 minutes, even intermittently; Exclusion Criteria: Patient : *…
Contacts

Nawale HADOUIRI

0380669073

nawale.hadouiri@chu-dijon.fr

CONTACT