Autosomal Dominant Polycystic Kidney Disease Somatic Mutation Biorepository
Part of paid clinical trials in New York, New York.
- Sponsor
- Weill Medical College of Cornell University
- Study ID
- NCT03901521
- Status
- Enrolling By Invitation
Conditions
- Autosomal Dominant Polycystic Kidney Disease
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 100 Years
- Healthy Volunteers
- Not accepted
Study Details
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 Dates
- Start date
- Jun 1, 2018
- Status verified
- Jan 2026
- Primary completion
- Dec 31, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 100 participants (estimated)
Primary Outcome Measure
The presence of somatic PKD 1/2 gene mutations in cyst epithelial cells [ Time Frame: 10 YEARS ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Weill Cornell Medicine | New York | New York | 10021 | - |
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