Mannosidase Deficiency Diseases

Explore clinical trials studying Mannosidase Deficiency Diseases. Study availability and eligibility vary by location and protocol.

18 public trials 6 recruiting studies

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Mannosidase Deficiency Diseases trial results

Completed

NCT02478840

Conditions: Alpha-Mannosidosis, Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +7 more
Locations: Center for Metabolic Diseases, Department of Clinical Genetics, Juliane Marie Centre, Copenhagen University Hospital, Blegdamsvej 9 Copenhagen, Denmark

Completed

NCT01681953

Conditions: Alpha-Mannosidosis, Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +7 more
Locations: Center for Metabolic Diseases, Department of Clinical Genetics, Juliane Marie Centre, Copenhagen University Hospital, Blegdamsvej 9 Copenhagen, Denmark

Hôpital Femme Mère Enfant, Lyon, 59 boulevard Pinel Bron, France

Hôpital Trousseau, Service de neuropédiatrie, Centre Référence des Maladies Lysosomales, 26 avenue du Docteur Arnold Netter Paris, France

Universitätsmedizin Mainz, Zentrum für Kinder- und Jugendmedizin, Langenbeckstrasse 1 Mainz, Germany

Completed

NCT01268358

Conditions: Alpha Mannosidosis, Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +7 more
Locations: Not specified

Completed

NCT00498420

Conditions: Alpha Mannosidosis, Bone Diseases, Bone Diseases, Developmental, +15 more
Locations: Department of Pediatrics, Charles University Prague, Czechia

University of Mainz Mainz, Germany

Department of Medicine, University of Tromsoe Tromsø, Norway

Willink Biochemical Genetics Unit,. Royal Manchester Children's Hospital Manchester, United Kingdom

Completed

NCT02141503

Conditions: Alpha-Mannosidosis, Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +7 more
Locations: National Institutes of Health Clinical Center, 9000 Rockville Pike Bethesda, Maryland, United States

Completed

NCT01043640

Conditions: Adrenal Gland Diseases, Adrenal Insufficiency, Adrenoleukodystrophy, +52 more
Locations: Masonic Cancer Center, University of Minnesota Minneapolis, Minnesota, United States

Completed

NCT01681940

Conditions: Alpha-Mannosidosis, Carbohydrate Metabolism, Inborn Errors, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +7 more
Locations: Kinderneurologie Metabole Ziekten, UZ Brussel, Laarbeeklaan 101 Brussels, Belgium

Center for Metabolic Diseases, Department of Clinical Genetics, Juliane Marie Centre, Copenhagen University Hospital, Blegdamsvej 9 Copenhagen, Denmark

Servicio de Pediatría, Hospital Materno Infantil, Reina Sofía, Avda Menéndez Pidal sn Córdoba, Spain

Genetic Medicine, 6th floor, St Mary's Hospital, Oxford Road, Manchester, United Kingdom

Active, Not Recruiting

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