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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
Identification of Women With Severe Insulin Resistant Syndromes of Genetic Origin Among Patients With "Classic" Polycystic Ovary Syndrome (PCOS)Adnexal Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cysts, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Genital Diseases, Lipid Metabolism Disorders, Lipid Metabolism, Inborn Errors, Nutritional and Metabolic Diseases, Skin Diseases, Metabolic, Skin and Connective Tissue Diseases, Urogenital Diseases, endocrine system disorder, familial partial lipodystrophy, female reproductive system disorder, gonadal disorder, hereditary disease, laminopathy, lipodystrophy, metabolic disease, neoplasm, ovarian cyst, ovarian disorder, polycystic ovary syndrome, skin disorderRecruitingNot applicable2026-08-10NCT07412028

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OrganizationsLinked trials
Assistance Publique - Hôpitaux de Paris985

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Research sitesCityCountryLinked trials
Service Endocrinologie, Hôpital St AntoineParisFrance1