Clin2
NCT05843851Possibly a fitRecruiting

Newborn screening for rare cystinosis and hyperoxaluria

CystinosisPrimary Hyperoxaluria

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

This study offers genetic screening to newborns to look for two rare metabolic conditions. It helps doctors find these conditions earlier, so treatment can start sooner if needed.

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

Phase
N/A
Enrollment
200,000 people
Ages
1 day to 3 days
Study type
Interventional

Who can take part

  • Be a newborn enrolled in the study’s genetic newborn screening program
  • Have a parent or guardian provide consent for the screening
  • Participate at the study site or through the program’s newborn screening process

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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