Massive study launches to map the course of rare muscle diseases
NCT ID NCT05989620
Summary
This study aims to better understand how several rare types of muscular dystrophy progress over time. Researchers will observe up to 1,000 participants for two years, tracking their strength, movement, and quality of life using standard tests and questionnaires. The goal is to gather detailed information to help design better future clinical trials for new treatments.
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.
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for LGMD2I are added.
By submitting, you agree to our Terms of use
Contacts and locations
Show contact details
Enter your email to view the contact information for this study.
By submitting, you agree to our Terms of use
Study contacts
-
Contact
Phone: •••-•••-•••• Email: •••••@•••••
-
Contact
Email: •••••@•••••
Locations
-
Virginia Commonwealth University
RECRUITINGRichmond, Virginia, 23298, United States
Contact Email: •••••@•••••
Contact
Conditions
Explore the condition pages connected to this study.