Clin2
NCT06900153Likely a fitRecruiting

Parenting in adults with CAH (21-hydroxylase deficiency)

CAH - 21-Hydroxylase Deficiency

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

This study looks at parenting in adults with congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency. It aims to understand how the condition affects family life so doctors can offer better support.

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

Phase
N/A
Enrollment
200 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You must be 18 or older.
  • You must have a confirmed diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency (a genetic condition).
  • You must be willing to participate and have been informed about the study.
  • You must speak French.
  • You must be covered by French social security (or be eligible for it).
  • You must not be under any legal protection, guardianship, or trusteeship.

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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