MYOTONIC DYSTROPHY, CONGENITAL
Clinical trials for MYOTONIC DYSTROPHY, CONGENITAL explained in plain language.
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Music sessions tested as therapy for rare muscle disease
Symptom relief Recruiting nowThis study explores whether weekly music and movement classes are practical and enjoyable for children aged 6–18 with myotonic dystrophy type 1 (DM1). Over 10 weeks, 13 participants will attend 45-minute sessions, wear activity trackers, and provide biological samples. The goal i…
Matched conditions: MYOTONIC DYSTROPHY, CONGENITAL
Phase: NA • Sponsor: Hanns Lochmuller • Aim: Symptom relief
Last updated May 26, 2026 04:37 UTC
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Spain launches massive DM1 registry to unlock disease secrets
Knowledge-focused Recruiting nowThis study aims to create a comprehensive national registry for Myotonic Dystrophy Type 1 (DM1) in Spain, collecting clinical, genetic, and protein data from 3,000 participants. By gathering detailed information, researchers hope to better understand the disease and identify peop…
Matched conditions: MYOTONIC DYSTROPHY, CONGENITAL
Sponsor: Fundació Institut Germans Trias i Pujol • Aim: Knowledge-focused
Last updated May 20, 2026 11:55 UTC