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Recruiting

NCT Number: NCT00792155

Polycystic Kidney Disease Data Repository

Autosomal dominant polycystic kidney disease (PKD) is the most common inherited kidney disease, affecting more than 400,000 people in the U.S. and 5 million people worldwide. PKD is the 4th most common cause of kidney failure requiring dialysis and/or transplantation. Over half of all PKD patients develop kidney failure by age 60 years, although age of onset of kidney disease varies widely, even among members of the same family.

Despite the fact this is a relatively common problem, relatively few patients have been studied for a sufficient period of time to fully understand how patients are affected over the course of their lifetime. The reason for creating this repository is to collect information about PKD so that the investigators may fully understand its complications, including high blood pressure, heart attack, and stroke. This information may also aid in the development of improved treatment strategies.

Recruiting

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Key information

About this study

Visit #1:

  • An initial detailed history, physical examination, and laboratory evaluation
  • An extensive family history of PKD will be obtained from the patient.

Follow-up Study Visits:

  • Patients will return to the outpatient facility for detailed follow-up examinations every other year after Visit 1.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Any person, age 18 or older, with previously diagnosed ADPKD is eligible to participate.

Exclusion criteria

  • Inability to provide informed consent.

Treatment and study plan

Primary outcomes

  1. Polycystic kidney disdease data repository

    Time frame: 30 years

    Polycystic kidney disease data repository

Study contacts

Contact information is provided by the study sponsor or research team.

Jon Blumenfeld, MD

CONTACT

[email protected]

212-746-1553

Sponsors and collaborators

Lead sponsor

The Rogosin Institute

Other

Collaborators

  • New York Presbyterian Hospital
  • Weill Medical College of Cornell University

Registry information

Official study title

Autosomal Dominant Polycystic Kidney Disease Data Repository

Important dates

Study start
2002
Primary completion
2030
Study completion
2030
First posted
Nov 17, 2008
Registry last updated
Nov 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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