NCT03513328
- Conditions
- Acquired Anemia Hemolytic, Acquired Neutropenia in Newborn, Acquired Thrombocytopenia, +82 more
- Locations
-
- UF Health Shands Children's Hospital Gainesville, Florida, United States
Clinical trial condition
Hurler Syndrome
Explore clinical trials studying Hurler Syndrome. Study availability and eligibility vary by location and protocol.
10 public trials
0 recruiting studies
Hurler Syndrome trial results
NCT01173016
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +10 more
- Locations
-
- Masonic Cancer Center, University of Minnesota Minneapolis, Minnesota, United States
NCT01917708
- Conditions
- Albinism, Anemia, Anemia, Aplastic, +80 more
- Locations
-
- Children's Healthcare of Atlanta Atlanta, Georgia, United States
Completed
Neurobehavioral Phenotypes in MPS III
NCT01873911
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Cognition Disorders, Cognitive Dysfunction, +17 more
- Locations
-
- University of Minnesota Minneapolis, Minnesota, United States
NCT00176891
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +10 more
- Locations
-
- Masonic Cancer Center, University of Minnesota Minneapolis, Minnesota, United States
NCT00638547
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +10 more
- Locations
-
- University of Minnesota, Fairview Minneapolis, Minnesota, United States
NCT01043640
- Conditions
- Adrenal Gland Diseases, Adrenal Insufficiency, Adrenoleukodystrophy, +52 more
- Locations
-
- Masonic Cancer Center, University of Minnesota Minneapolis, Minnesota, United States
NCT00146757
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +12 more
- Locations
-
- Hôpital E. Herriot Lyon, France
- Johannes Gutenberg Universität Kinderklinik, Mainz, Germany
- Sophia Children's Hospital Rotterdam, Netherlands
- Willink Biochemical Genetics Unit Royal Hospital for Children Manchester, United Kingdom
Completed
Study of Aldurazyme® Replacement Therapy in Patients With Mucopolysaccharidosis I (MPS I) Disease
NCT00258011
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +12 more
- Locations
-
- Osaka City University Hospital Osaka, Japan
- National Center for Child Health and Development Tokyo, Japan
Active, Not Recruiting
MT2013-31: Allo HCT for Metabolic Disorders and Severe Osteopetrosis
NCT02171104
- Conditions
- Abnormalities, Multiple, Acyl-CoA Oxidase Deficiency, Adrenoleukodystrophy With Cerebral Involvement, +85 more
- Locations
-
- Masonic Cancer Center, University of Minnesota Minneapolis, Minnesota, United States