Repository Study of Autosomal Dominant Polycystic Kidney Disease

NCT01988038 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2017-03-29

No results posted yet for this study

Summary

The design and establishment of the Polycystic Kidney Disease (PKD) Data Repository does not require, and may be constrained by, a narrowly conceived hypothesis. However, the PKD Repository has been designed to include demographic, clinical, biochemical, and genetic data that will further explore the natural history of the disorder and assess the factors that are likely to be associated with the progression of disease and the incidence of complications including renal failure, cardiovascular disease, and stroke.

Conditions

  • Autosomal Dominant Polycystic Kidney Disease

Sponsors & Collaborators

  • Weill Medical College of Cornell University

    collaborator OTHER
  • New York Presbyterian Hospital

    collaborator OTHER
  • The Rogosin Institute

    lead OTHER

Principal Investigators

  • Jon Blumenfeld, MD · The Rogosin Institute

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2016-06-30
Completion
2016-06-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01988038 on ClinicalTrials.gov