Completed
TyG Index Levels in Klinefelter Syndrome
NCT05014997
- Conditions
- Cardiac Event, Cardiovascular Diseases, Chromosome Disorders, +16 more
- Locations
-
Not specified
Clinical trial condition
Sex Chromosome Disorders
Explore clinical trials studying Sex Chromosome Disorders. Study availability and eligibility vary by location and protocol.
215 public trials
41 recruiting studies
Sex Chromosome Disorders trial results
NCT01585831
- Conditions
- Chromosome Aberrations, Chromosome Disorders, Congenital Abnormalities, +18 more
- Locations
-
- Childrens Hospital Colorado Aurora, Colorado, United States
Completed
RA-2 13-cis Retinoic Acid (Isotretinoin)
NCT02061384
- Conditions
- Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +21 more
- Locations
-
- University of Washington Medical Center Seattle, Washington, United States
NCT00348946
- Conditions
- Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +13 more
- Locations
-
- Thomas Jefferson University, Department of Pediatrics, 1025 Walnut Street, Suite 726 Philadelphia, Pennsylvania, United States
NCT03624556
- Conditions
- Abnormalities, Multiple, Chromosome Disorders, Congenital Abnormalities, +16 more
- Locations
-
- IMIM (Institut Hospital del Mar d'Investigacions Mèdiques) Barcelona, Spain
NCT03181230
- Conditions
- Cardiovascular Abnormalities, Cardiovascular Diseases, Chromosome Disorders, +20 more
- Locations
-
- Children's Hospital Colorado Aurora, Colorado, United States
NCT03140813
- Conditions
- Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
- Locations
-
- Cincinnati Children's Hospital Medical Center Cincinnati, Ohio, United States
NCT03722290
- Conditions
- Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
- Locations
-
- Université de Sherbrooke Sherbrooke, Quebec, Canada
NCT01911455
- Conditions
- Chromosome Disorders, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +10 more
- Locations
-
- Rush University Medical Center Chicago, Illinois, United States
- Cincinnati Children's Hospital Medical Center Cincinnati, Ohio, United States
NCT02381457
- Conditions
- 1p36 Deletion Syndrome, 22q11 Deletion Syndrome, Abnormalities, Multiple, +58 more
- Locations
-
- University of California, San Francisco San Francisco, California, United States
- Cooper University Hospital Camden, New Jersey, United States
- Virtua Mount Laurel, New Jersey, United States
- St. Peter's University New Brunswick, New Jersey, United States
Related conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities (215)
- Chromosome Disorders (213)
- Congenital Abnormalities (211)
- Genetic Diseases, Inborn (197)
- Endocrine System Diseases (131)
- Female Urogenital Diseases (129)
- Female Urogenital Diseases and Pregnancy Complications (129)
- Male Urogenital Diseases (129)