Patients unite to map a rare kidney disease
NCT ID NCT00481130
Summary
This study created a central registry of 655 patients and families affected by Alport syndrome, a rare genetic kidney disease. The goal was to collect information to better understand the disease and to help plan future research into potential treatments. It did not test any treatments itself but gathered data to serve as a foundation for future clinical trials.
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Contacts and locations
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Locations
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University of Minnesota
Minneapolis, Minnesota, 55455, United States
Conditions
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