Service d'endocrinologie, Hôpital Pitié Salpêtrière

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Parenting and CAH - 21-hydroxylase Deficiency	Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Male Urogenital Diseases, Nutritional and Metabolic Diseases, Urogenital Abnormalities, Urogenital Diseases, adrenal gland disorder, adrenogenital syndrome, congenital adrenal hyperplasia, disorder of sexual differentiation, endocrine system disorder, gonadal disorder, hereditary disease, inborn errors of metabolism, metabolic disease, steroid inherited metabolic disorder	Recruiting	Not stated	2026-08-31		NCT06900153

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