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NCT04338048Recruiting

Autosomal Dominant Polycystic Kidney Disease (ADPKD) Study

Source: ClinicalTrials.gov · Last updated 15 Jun 2026

Brief summary (registry, in English)

Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common genetic cause of renal failure. For several decades, ADPKD was regarded as an adult-onset disease. In the last decade, it has become more widely appreciated that the disease course begins in childhood. However, evidence-based guidelines on how to manage and approach children diagnosed with or at-risk for of ADPKD are lacking. Overall, there is insufficient data on the clinical course during childhood. The study intends to get more information on Autosomal Dominant Polycystic Kidney Disease (ADPKD) and other hepato/renal fibrocystic diseases. Additionally, the study intends to expand web-based resources so anyone can learn about ADPKD or other hepato/renal fibrocystic diseases. Individuals diagnosed with the dominant form of a hepato/renal fibrocystic condition are invited to be in the study.

Status (registry)
Recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
2 Jan 2020
Start date
10 Oct 2019
Primary completion date
30 Oct 2030
Lead sponsor
Children's Hospital of Philadelphia
NCT number
NCT04338048

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From 10 Oct 2019 to the primary completion date, 30 Oct 2030
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with Autosomal Recessive Polycystic Kidney disease (ARPKD), urinary tract malformations or major congenital anomalies of other systems suggesting a diagnosis other than recessive hepato-renal fibrocystic diseases.

Who the study is looking for

  • Demonstration of ADPKD by clinical information, imaging studies, biopsy, autopsy, or genetic testing.

Age in the registry: - to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cohen Children's Medical Center
Coordinator of this site? Confirm its status
New Hyde ParkUnited StatesEnrolling by invitation
Children's Hospital of Philadelphia
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesRecruiting
Mayo Clinic
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting
Children's National Hospital
Coordinator of this site? Confirm its status
Washington D.C.United StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.