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ENROLLING BY INVITATION
NCT03901521
Autosomal Dominant Polycystic Kidney Disease Somatic Mutation Biorepository
Sponsor: Weill Medical College of Cornell University
View on ClinicalTrials.gov
Summary
This study will analyze the germline and somatic mutations underlying the development of ADPKD in order to better understand the genetic mechanism responsible for the cystic transformation. Once identified, these mutations could help us understand better the mechanism leading to the development of this disease and may explain at least in part the phenotypic variability.
Key Details
Gender
All
Age Range
18 Years - 100 Years
Study Type
OBSERVATIONAL
Enrollment
100
Start Date
2018-06-01
Completion Date
2028-12-31
Last Updated
2026-01-22
Healthy Volunteers
No
Locations (1)
Weill Cornell Medicine
New York, New York, United States