NCT06682078
- Conditions
- Androgen-Insensitivity Syndrome, Anorchia, Congenital Abnormalities, +22 more
- Locations
-
- Service de Chirurgie uro-viscérale pédiatrique Bron, France
Clinical trial condition
Disorder of Sex Development, 46,XY
Explore clinical trials studying Disorder of Sex Development, 46,XY. Study availability and eligibility vary by location and protocol.
23 public trials
6 recruiting studies
Disorder of Sex Development, 46,XY trial results
Completed
Kisspeptin Administration in the Adult
NCT00914823
- Conditions
- Adnexal Diseases, Brain Diseases, Central Nervous System Diseases, +30 more
- Locations
-
- Massachusetts General Hospital Boston, Massachusetts, United States
NCT01438034
- Conditions
- Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Delayed Puberty, +15 more
- Locations
-
- Massachusetts General Hospital Boston, Massachusetts, United States
NCT00392756
- Conditions
- Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disorder of Sex Development, 46,XY, +13 more
- Locations
-
- Massachusetts General Hospital Boston, Massachusetts, United States
NCT00493961
- Conditions
- Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disorder of Sex Development, 46,XY, +13 more
- Locations
-
- Massachusetts General Hospital Boston, Massachusetts, United States
NCT00494169
- Conditions
- Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disorder of Sex Development, 46,XY, +16 more
- Locations
-
- Massachusetts General Hospital Boston, Massachusetts, United States
NCT00758108
- Conditions
- Aniridia, Behavior, Body Weight, +45 more
- Locations
-
- National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States
NCT01914172
- Conditions
- Congenital Abnormalities, Congenital Hypogonadotropic Hypogonadism, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +17 more
- Locations
-
- Centre Hospitalier Universitaire Vaudois (CHUV) Lausanne, Canton of Vaud, Switzerland
Completed
Registry for Patients With Wilms' Tumor Suppressor Gene 1 (WT1) Mutation Associated Diseases
NCT01252901
- Conditions
- Chronic Disease, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +35 more
- Locations
-
- Universitätskrankenhaus Hamburg-Eppendorf Hamburg, Germany
NCT00392457
- Conditions
- Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disorder of Sex Development, 46,XY, +13 more
- Locations
-
- Massachusetts General Hospital Boston, Massachusetts, United States
Related conditions
- Congenital Abnormalities (23)
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities (23)
- Female Urogenital Diseases (23)
- Female Urogenital Diseases and Pregnancy Complications (23)
- Male Urogenital Diseases (23)
- Urogenital Diseases (23)
- Disorders of Sex Development (22)
- Endocrine System Diseases (22)