Clin2
NCT06979024Likely a fitEnrolling by invitation

Observational study of myotonic dystrophy type 1

Myotonic Dystrophy Type 1 (DM1)

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital clinical trials.

This study follows people with myotonic dystrophy type 1 over time to learn more about the condition. It is for people of any age who have genetic confirmation of DM1, whether or not they have symptoms.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
300 people
Ages
Any age
Study type
Observational

Who can take part

  • You must have a genetic test result that confirms you have myotonic dystrophy type 1 (DM1).
  • You can have symptoms or not — either is fine.
  • You cannot have another muscle disease, like limb-girdle muscular dystrophy.
  • You should not have a serious health problem like heart, liver, or kidney disease or a major mental illness.
  • You must be willing to join the study.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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