The Spanish National Registry for Myotonic Dystrophy Type 1

Recruiting Observational Study
Myotonic Dystrophy 1 DM1 Myotonic Dystrophy Type 1 Myotonic Dystrophy, Congenital Steinert Disease
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Sex
Any
Study type
Observational
Participants needed
3,000 (estimated)
Sponsor
Fundació Institut Germans Trias i Pujol · Other
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About This Trial
Myotonic Dystrophy Type 1 (DM1) is a rare genetic neuromuscular condition that can affect multiple organs and varies widely in how it presents. DM1 is the most common form of adult-onset muscular dystrophy, with an estimated prevalence of approximately 1-5 per 10,000 people. In Spain, the condition shows notable regional differences, making it especially important to understand its characteristics…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Confirmed diagnosis of Myotonic Dystrophy Type 1 (DM1) through genetic testing. Exclusion Criteria: * There are no exclusion criteria for the registry
Contacts

Gisela Nogales Gadea, Ph.D.

(+34) 93 554 3050

gnogales@igtp.cat

CONTACT

Alvaro S Larran Mottino, Ph.D.

alarran@igtp.cat

CONTACT