CONGENITAL MYOTONIC DYSTROPHY
Clinical trials for CONGENITAL MYOTONIC DYSTROPHY explained in plain language.
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Scientists hunt for biomarkers to unlock DM1 treatments
Knowledge-focused Recruiting nowThis study follows 1,000 adults with myotonic dystrophy type 1 (DM1) over time to measure how the disease progresses. Researchers will track walking speed, hand muscle relaxation, grip strength, heart and lung function, and daily activity. The goal is to establish reliable biomar…
Matched conditions: CONGENITAL MYOTONIC DYSTROPHY
Sponsor: Virginia Commonwealth University • Aim: Knowledge-focused
Last updated Jul 15, 2026 00:00 UTC
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New study aims to improve monitoring of rare childhood muscle disease
Knowledge-focused Recruiting nowThis study is for children up to 4 years old with congenital myotonic dystrophy type 1 (CDM). Researchers want to find better ways to measure how the disease affects motor skills and language, and to identify biological markers. The goal is to improve future clinical trials and c…
Matched conditions: CONGENITAL MYOTONIC DYSTROPHY
Sponsor: Virginia Commonwealth University • Aim: Knowledge-focused
Last updated Jun 27, 2026 13:06 UTC
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Join the fight: new registry connects muscle disease patients with scientists
Knowledge-focused Recruiting nowThis registry aims to connect people diagnosed with myotonic dystrophy (DM) or facioscapulohumeral muscular dystrophy (FSHD) with researchers. By joining, participants help scientists better understand these inherited muscle-weakening diseases and develop future treatments. The r…
Matched conditions: CONGENITAL MYOTONIC DYSTROPHY
Sponsor: University of Rochester • Aim: Knowledge-focused
Last updated Jun 27, 2026 07:54 UTC