Clin2
NCT00792155Likely a fitRecruiting

Register people with diagnosed ADPKD to build a kidney data resource

Polycystic Kidney Disease

Part of Genetic & congenital, Kidney & urinary, Women’s health & pregnancy clinical trials.

This trial builds a secure database by collecting information from adults who already have autosomal dominant polycystic kidney disease (ADPKD). Your information can help researchers understand the condition better and improve future care.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
1,000 people
Ages
18 years and older
Study type
Observational

Who can take part

  • Be 18 years or older
  • Have a previous diagnosis of ADPKD
  • Be able to understand and agree to the study (informed consent)
  • Plan to participate in providing study information for the data repository

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT01873235Recruiting
Study for adults with confirmed polycystic kidney disease

This study enrolls adults with autosomal dominant polycystic kidney disease (ADPKD) to better understand the disease and its related changes in the body. It may help researchers find improved ways to track the condition and support future treatments.

Baltimore, Maryland
NCT02936791Recruiting
Study of early inherited kidney cysts and healthy volunteers

This observational study follows people early in autosomal dominant polycystic kidney disease (ADPKD) and also some healthy volunteers to learn how the kidneys work over time. It may help researchers understand early changes, which could guide future treatments.

Chicago, Illinois
NCT03901521Enrolling by invitation
Biobank for people with autosomal dominant polycystic kidney disease

This study collects samples and health information from adults with autosomal dominant polycystic kidney disease (ADPKD) who are having their own kidney removed. It helps researchers learn more about ADPKD and its genetic changes to support future treatments.

New York, New York
NCT04039061Recruiting
Study registry for people with ADPKD

This trial is a patient registry that collects information from people who have—or might have—autosomal dominant polycystic kidney disease (ADPKD). It may help researchers better understand the condition and improve future studies.

Kansas City, Missouri
NCT06759142Recruiting
Study of people with ADPKD

This study looks at people with autosomal dominant polycystic kidney disease to learn more about the condition. It is an observational study, meaning no new treatments are tested—just gathering information from your medical history and tests.

Bologna
NCT04338048Recruiting
Study for autosomal dominant polycystic kidney disease

This study enrolls people who have been diagnosed with autosomal dominant polycystic kidney disease (ADPKD), a genetic kidney condition that can cause kidney cysts. It aims to learn about this specific form of the disease so better care is possible for the right patients.

Washington D.C., District of Columbia

Hear when a new Polycystic Kidney Disease trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.