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Simple blood test may predict muscle disease severity

NCT ID NCT07415837

First seen Mar 01, 2026 · Last updated Jun 22, 2026 · Updated 15 times

Summary

This study is looking at whether a molecule in the blood called miR-1 can help doctors understand how muscle diseases like Duchenne muscular dystrophy and myotonic dystrophy are progressing. Researchers will compare miR-1 levels in 104 people, including patients with different muscle conditions and healthy volunteers. The goal is to see if miR-1 levels match how severe the disease is, which could lead to a simple blood test for monitoring these conditions.

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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

  • CHU de Clermont-Ferrand

    RECRUITING

    Clermont-Ferrand, France

    Contact

    Contact Email: •••••@•••••

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to

If successful, this could lead to a simple blood test to monitor muscle disease progression, helping doctors adjust treatments earlier.

What could go wrong

This is an early observational study, not a treatment trial. It may find that miR-1 levels do not reliably reflect disease severity, or results may not apply to all muscle conditions.

Conditions

The condition(s) this trial relates to.

Becker muscular dystrophy congenital myopathy Duchenne muscular dystrophy myotonic dystrophy myotonic dystrophy type 1 neuromuscular disease Thomsen and Becker disease

As listed by the trial registrant

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