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 in kids
Symptom relief Recruiting nowThis study explores whether weekly music and movement sessions are practical and enjoyable for children aged 6 to 18 with myotonic dystrophy type 1 (DM1). Over 10 weeks, participants attend 45-minute music classes, undergo physical and cognitive tests, and provide biological samp…
Matched conditions: MYOTONIC DYSTROPHY, CONGENITAL
Phase: NA • Sponsor: Hanns Lochmuller • Aim: Symptom relief
Last updated May 17, 2026 08:25 UTC
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Massive spanish DM1 registry aims to unlock disease secrets
Knowledge-focused Recruiting nowThis study is creating a large national registry in Spain for people with Myotonic Dystrophy Type 1 (DM1), a rare genetic muscle disease. Researchers will collect medical information, genetic data, and patient reports from up to 3,000 participants. The goal is to better understan…
Matched conditions: MYOTONIC DYSTROPHY, CONGENITAL
Sponsor: Fundació Institut Germans Trias i Pujol • Aim: Knowledge-focused
Last updated May 17, 2026 08:32 UTC