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No travel needed: new study aims to unlock secrets of myotonic dystrophy

NCT ID NCT07505342

First seen Apr 02, 2026 · Last updated Jun 05, 2026 · Updated 13 times

Summary

This study looks at why myotonic dystrophy type 1 affects people so differently—some have mild symptoms, others severe. Researchers will measure muscle strength, memory, and activity using tools mailed to your home, plus analyze your DNA from a blood sample. The goal is to find better ways to track the disease and understand its genetic causes.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • University of Rochester

    RECRUITING

    Rochester, New York, 14642, United States

    Contact Phone: •••-•••-•••• Email: •••••@•••••

    Contact

Conditions

The condition(s) this trial relates to.

myotonic dystrophy

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.