Rare muscle disease study aims to pave way for future treatments

NCT ID NCT07201636

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study follows up to 10 people of any age with nemaline myopathy, a rare muscle disease, for three years. Researchers will collect information during regular hospital visits to understand how the disease changes over time. The goal is to find better ways to measure disease progression, which can help design future clinical trials for potential treatments.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Centre de référence des maladies neuromusculaire, Centre Hospitalier Régional de la Citadelle

    Liège, 4000, Belgium

More trials for these conditions

Other studies related to the condition(s) this trial covers.