NCT02819037
- Conditions
- Bacterial Overgrowth Syndrome, Blind Loop Syndrome, Carbohydrate Metabolism, Inborn Errors, +17 more
- Locations
-
- Centre Hospitalier d'Arras Arras, France
- Centre Hospitalier de Douai Douai, France
Clinical trial condition
Mucopolysaccharidoses
Explore clinical trials studying Mucopolysaccharidoses. Study availability and eligibility vary by location and protocol.
193 public trials
26 recruiting studies
Mucopolysaccharidoses trial results
NCT04759885
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +10 more
- Locations
-
- Centre Hospitalier Henri Duffaut Avignon, France
- Hospices civils de Lyon Lyon, France
- Hôpital Edouard Herriot Lyon, France
- Centre Hospitalier Universitaire de Montpellier Montpellier, France
NCT04265651
- Conditions
- Achondroplasia, Bone Diseases, Bone Diseases, Developmental, +16 more
- Locations
-
- UCSF Benioff Children's Hospital Oakland, California, United States
- Nemours Alfred I. Dupont Hospital for Children Wilmington, Delaware, United States
- Johns Hopkins School of Medicine Baltimore, Maryland, United States
- Cincinnati Children's Hospital Medical Center Cincinnati, Ohio, United States
NCT03204370
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +10 more
- Locations
-
- Rheumatology department - Bordeaux University Hospital Bordeaux, Aquitaine, France
NCT05134571
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +9 more
- Locations
-
- Investigational Site Number :1560003 Beijing, China
- Investigational Site Number :1560002 Beijing, China
- Investigational Site Number :1560004 Guangzhou, China
- Investigational Site Number :1560006 Hangzhou, China
Completed
An Extension Study of JR-171-101 Study in Patients With Mucopolysaccharidosis Type I (MPS I)
NCT04453085
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +9 more
- Locations
-
- UCSF Benioff Children's Hospital Oakland Oakland, California, United States
- Hospital de Clínicas de Porto Alegre Porto Alegre, Brazil
- Instituto de Genética e Erros Inatos do Metabolismo - IGEIM São Paulo, Brazil
- Fukuoka Children's Hospital Fukuoka, Japan
Completed
Baby Detect : Genomic Newborn Screening
NCT05687474
- Conditions
- 3-Hydroxy 3-Methyl Glutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, 3-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency, +368 more
- Locations
-
- CRMN, Hôpital La Citadelle Liège, Wallonia, Belgium
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +23 more
- Locations
-
- Ann & Robert H Lurie Childrens Hospital of Chicago Chicago, Illinois, United States
- University of North Carolina at Chapel Hill Chapel Hill, North Carolina, United States
- Legacy Emanuel Hospital Portland, Oregon, United States
- Children's Hospital of Pittsburgh of UPMC Pittsburgh, Pennsylvania, United States
NCT03359213
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +16 more
- Locations
-
- Grupo de Pesquisa Clínica em Genética Médica - HCPA Porto Alegre, Brazil
- Igeim - Unifesp São Paulo, Brazil
NCT06064656
- Conditions
- Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Connective Tissue Diseases, +17 more
- Locations
-
- Regeneron Tarrytown, New York, United States
Related conditions
- Carbohydrate Metabolism, Inborn Errors (193)
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities (193)
- Mucinoses (193)
- Nutritional and Metabolic Diseases (193)
- Skin and Connective Tissue Diseases (193)
- Connective Tissue Diseases (192)
- Metabolic Diseases (189)
- Metabolism, Inborn Errors (187)