Early PKD Observational Cohort Study
Part of paid clinical trials in Chicago, Illinois.
- Sponsor
- University of Kansas Medical Center
- Study ID
- NCT02936791
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 4 Years - 35 Years
- Healthy Volunteers
- Accepted
Study Details
This observational study will collect blood and urine and clinical information from individuals with early-stages of polycystic kidney disease (PKD), their unaffected siblings and normal volunteers to create a biobank, also called a biorepository. The long-term goal is to develop new knowledge on biological markers or biomarkers that indicate changes in the disease progression. An understanding of biomarkers for early renal cyst growth will benefit PKD patients as new therapies are being developed and tested.
Key Dates
- Start date
- Apr 30, 2016
- Status verified
- Apr 2026
- Primary completion
- Jun 30, 2030
- Completion
- Jun 30, 2031
Study Design
- Enrollment
- 250 participants (estimated)
Arms
- Arm: Individuals diagnosed with PKDIndividuals that have been diagnosed and meet the study's definition of early stage PKD.
- Arm: Individuals with a family history of PKDUnaffected/ undiagnosed family members, preferably siblings, of participants with PKD
- Arm: Normal individuals for the comparisonNormal volunteers with no family history of PKD or other kidney diseases.
Primary Outcome Measure
Collect blood and urine samples from affected and unaffected cohorts for basic and translational research [ Time Frame: 10 years ]
Central Contacts
- Cathy Creed, RN913-588-0053
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Chicago | Chicago | Illinois | 60637 | Arlene Chapman, MD Arlene Chapman, MD (PRINCIPAL_INVESTIGATOR) |
| University of Kansas Medical Center | Kansas City | Kansas | 66160 | |
| Children's Mercy Hospital | Kansas City | Missouri | 64108 | Laurel Willig, MD, MS (PRINCIPAL_INVESTIGATOR) |
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