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Mitochondrial neurogastrointestinal encephalopathy syndrome

Mitochondrial neurogastrointestinal encephalomyopathy syndromeMNGIE
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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-6 of 6 results.
MNGIE Allogeneic Hematopoietic Stem Cell Transplant Safety Study
Status: Recruiting
Last Changed: Aug 05, 2019
First Received: Apr 27, 2015
Disease(s): Mitochondrial Neurogastrointestinal Encephalomyopathy (MNGIE)
Intervention(s): Hematopoietic Allogeneic Stem Cells
Locations: Columbia University, New York, New York, United States
The Natural History Study of Mitochondrial NeuroGastroIntestinal Encephalopathy (MNGIE)
Status: Recruiting
Last Changed: Feb 27, 2019
First Received: Sep 27, 2012
Disease(s): Mitochondrial NeuroGastroIntestinal Encephalopathy (MNGIE)
Locations: Columbia University, New York, New York, United States
Natural History Study of MNGIE
Status: Not yet recruiting
Last Changed: Jan 29, 2020
First Received: Jan 29, 2020
Disease(s): Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome
Intervention(s): Non-interventional
Trial of Erythrocyte Encapsulated Thymidine Phosphorylase In Mitochondrial Neurogastrointestinal Encephalomyopathy
Status: Not yet recruiting
Last Changed: Nov 05, 2019
First Received: Mar 07, 2019
Disease(s): Mitochondrial Diseases, Metabolic Disease, Inborn Errors of Metabolism
Intervention(s): EE-TP
MT2013-31: Allo HCT for Metabolic Disorders and Severe Osteopetrosis
Status: Recruiting
Last Changed: Sep 26, 2019
First Received: Jun 23, 2014
Disease(s): Mucopolysaccharidosis Disorders, Hurler Syndrome, Hunter Syndrome, Maroteaux Lamy Syndrome, Sly Syndrome, Alpha-Mannosidosis, Fucosidosis, Aspartylglucosaminuria, Glycoprotein Metabolic Disorders, Sphingolipidoses, Recessive Leukodystrophies, Globoid Cell Leukodystrophy, Metachromatic Leukodystrophy, Niemann-Pick B, Niemann-Pick C Subtype 2, Sphingomyelin Deficiency, Peroxisomal Disorders, Adrenoleukodystrophy With Cerebral Involvement, Zellweger Syndrome, Neonatal Adrenoleukodystrophy, Infantile Refsum Disease, Acyl-CoA Oxidase Deficiency, D-Bifunctional Enzyme Deficiency, Multifunctional Enzyme Deficiency, Alpha-methylacyl-CoA Racmase Deficiency, Mitochondrial Neurogastrointestingal Encephalopathy, Severe Osteopetrosis, Hereditary Leukoencephalopathy With Axonal Spheroids (HDLS; CSF1R Mutation), Inherited Metabolic Disorders
Intervention(s): Stem Cell Transplantation, IMD Preparative Regimen, Osteopetrosis Only Preparative Regimen, Osteopetrosis Haploidentical Only Preparative Regimen, cALD SR-A (Standard-Risk, Regimen A), cALD SR-B (Standard-Risk, Regimen B), cALD HR-D (High-Risk, Regimen C), cALD HR-D (High-Risk, Regimen D)
Locations: Masonic Cancer Center, University of Minnesota, Minneapolis, Minnesota, United States
North American Mitochondrial Disease Consortium Patient Registry and Biorepository (NAMDC)
Status: Recruiting
Last Changed: Aug 05, 2019
First Received: Sep 27, 2012
Disease(s): Mitochondrial Disorders, Mitochondrial Genetic Disorders, Mitochondrial Diseases, Disorder of Mitochondrial Respiratory Chain Complexes, Deletion and Duplication of Mitochondrial DNA
Locations: University of California San Diego, San Diego, California, United States
Lucile Packard Children's Hospital, Stanford, California, United States
Children's Hospital of Colorado, Aurora, Colorado, United States
Children's National Medical Center, Washington, District of Columbia, United States
University of Florida, Gainesville, Florida, United States
... and 13 other locations.