Register people with diagnosed ADPKD to build a kidney data resource
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.
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
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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