NCT03689621
- Conditions
- Abnormalities, Multiple, Chromosome Disorders, Congenital Abnormalities, +14 more
- Locations
-
Not specified
Clinical trial condition
Imprinting Disorders
Explore clinical trials studying Imprinting Disorders. Study availability and eligibility vary by location and protocol.
142 public trials
27 recruiting studies
Imprinting Disorders trial results
NCT03081832
- Conditions
- Abnormalities, Multiple, Chromosome Disorders, Congenital Abnormalities, +13 more
- Locations
-
- Centre de référence du syndrome de Prader-Willi Hôpital des Enfants Toulouse, France
NCT03673813
- Conditions
- Abnormalities, Multiple, Behavior, Chromosome Disorders, +27 more
- Locations
-
Not specified
NCT03565081
- Conditions
- Abnormalities, Multiple, Chromosome Disorders, Congenital Abnormalities, +14 more
- Locations
-
Not specified
Completed
Oxytocin Trial in Prader-Willi Syndrome
NCT02013258
- Conditions
- Abnormalities, Multiple, Chromosome Disorders, Congenital Abnormalities, +14 more
- Locations
-
- University of California, Irvine Orange, California, United States
- University of Florida Gainesville, Florida, United States
- University of Kansas Medical Center Kansas City, Kansas, United States
NCT02368379
- Conditions
- Abnormalities, Multiple, Adrenal Gland Diseases, Adrenal Insufficiency, +17 more
- Locations
-
- Nationwide Children's Hospital Columbus, Ohio, United States
Completed
Single Dose Pharmacokinetic (PK) Study
NCT03109756
- Conditions
- Abnormalities, Multiple, Angelman Syndrome, Central Nervous System Diseases, +15 more
- Locations
-
- Ovid Therapeutics Investigative Site Chicago, Illinois, United States
- Ovid Therapeutics Investigative Site Nashville, Tennessee, United States
NCT01038570
- Conditions
- Abnormalities, Multiple, Anxiety Disorders, Behavior, +18 more
- Locations
-
- Hôpital marin d'Hendaye Hendaye, Pyrénées-Atlantiques, France
NCT01401244
- Conditions
- Abnormalities, Multiple, Chromosome Disorders, Congenital Abnormalities, +20 more
- Locations
-
- Novo Nordisk Investigational Site Evansville, Indiana, United States
NCT01548521
- Conditions
- Abnormalities, Multiple, Chromosome Disorders, Congenital Abnormalities, +13 more
- Locations
-
- Children Hospital of Toulouse Purpan Toulouse, France