Clin2
NCT04947813Possibly a fitRecruiting

Study links Alport genetics to kidney symptoms

Alport Syndrome

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

This study looks at how specific genetic changes (genotypes) relate to kidney problems and urine blood findings in people with Alport syndrome. It may help doctors predict disease course and tailor care, though it may not involve new treatment.

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

Phase
N/A
Enrollment
8,165 people
Ages
Any age
Study type
Observational

Who can take part

  • Be any age (including children and older adults, up to age 99)
  • Have a history of blood in the urine from kidney problems (renal hematuria)
  • Have had Alport syndrome in your family or in your own history
  • Be able to sign the study consent form
  • Have enough past medical records and kidney test results to complete the study

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.

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