New study tracks liver risks in rare muscle disease
NCT ID NCT06581146
First seen Nov 01, 2025 · Last updated May 13, 2026 · Updated 24 times
Summary
This study follows about 50 boys under 18 with XLMTM, a serious genetic muscle condition, for one year to see how often liver and gallbladder problems occur. Researchers will collect health information and use a special liver scan (Fibroscan) at home or in clinic. The goal is to better understand these issues and improve routine care for affected children.
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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.
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
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Study contacts
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Contact
Phone: •••-•••-•••• Email: •••••@•••••
Locations
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Ann & Robert H. Lurie Children's Hospital of Chicago
RECRUITINGChicago, Illinois, 60611, United States
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Boston Children's Hospital
RECRUITINGBoston, Massachusetts, 02115, United States
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Children's Hospital of Philadelphia
RECRUITINGPhiladelphia, Pennsylvania, 19104, United States
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Cincinnati Children's Hospital Medical Center
RECRUITINGCincinnati, Ohio, 45229, United States
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UPMC Children's Hospital of Pittsburgh
RECRUITINGPittsburgh, Pennsylvania, 15224, United States
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University of Utah
RECRUITINGSalt Lake City, Utah, 84112, United States
Conditions
Explore the condition pages connected to this study.