congenital bilateral absence of vas deferens

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
Establishment of a Primary Epididymal Cell Model From Epididymal Samples to Study CFTR Gene Regulation	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Genital Diseases, Infant, Newborn, Diseases, Male Urogenital Diseases, Sterility, Male, Urogenital Diseases, congenital bilateral absence of vas deferens, cystic fibrosis, hereditary disease, infertility disorder, lung disorder, male infertility, male reproductive system disorder, pancreas disorder, respiratory system disorder	Recruiting	Not stated	2026-03-20		NCT06045702

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