NCT00004350
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cystinosis, Disease Attributes, +16 more
- Locations
-
Not specified
Clinical trial condition
Rare Diseases
Explore clinical trials studying Rare Diseases. Study availability and eligibility vary by location and protocol.
467 public trials
83 recruiting studies
Rare Diseases trial results
NCT00006058
- Conditions
- Bronchopulmonary Dysplasia, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, +11 more
- Locations
-
- Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States
Completed
Genetic Study of Familial Epilepsy
NCT00006059
- Conditions
- Brain Diseases, Central Nervous System Diseases, Disease Attributes, +9 more
- Locations
-
- Columbia University College of Physicians and Surgeons New York, United States
Completed
Phase IV Study of Chronic Infusional Epoprostenol for Severe Primary Pulmonary Hypertension
NCT00004754
- Conditions
- Cardiovascular Diseases, Disease Attributes, Familial Primary Pulmonary Hypertension, +8 more
- Locations
-
Not specified
NCT00004340
- Conditions
- Avitaminosis, Bone Diseases, Bone Diseases, Metabolic, +30 more
- Locations
-
- University of California Los Angeles School of Medicine Los Angeles, California, United States
Completed
Phase III Randomized Study of Ursodiol With Vs Without Methotrexate for Primary Biliary Cirrhosis
NCT00004784
- Conditions
- Bile Duct Diseases, Biliary Tract Diseases, Cholestasis, +11 more
- Locations
-
Not specified
NCT00004805
- Conditions
- Bronchopulmonary Dysplasia, Cardiovascular Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +17 more
- Locations
-
Not specified
NCT00004642
- Conditions
- Communicable Diseases, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cytomegalovirus Infections, +10 more
- Locations
-
Not specified
NCT00006137
- Conditions
- Autoimmune Diseases, Disease Attributes, Female Urogenital Diseases, +13 more
- Locations
-
Not specified
NCT00004785
- Conditions
- Bronchopulmonary Dysplasia, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, +9 more
- Locations
-
Not specified