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Ocular Muscular Dystrophy

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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-4 of 4 results.
Nicotinamide Riboside and Mitochondrial Biogenesis
Status: Recruiting
Last Changed: Jul 08, 2019
First Received: Feb 14, 2018
Disease(s): Mitochondrial Diseases, Mitochondrial Myopathies, Progressive External Ophthalmoplegia, Progressive Ophthalmoplegia, Progressive; Ophthalmoplegia, External, Mitochondria DNA Deletion, MELAS, Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes, Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS Syndrome)
Intervention(s): Nicotinamide Riboside
Locations: Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom
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.
Biomarker for Duchenne Muscular Dystrophy
Status: Recruiting
Last Changed: Apr 30, 2020
First Received: Dec 15, 2016
Disease(s): Increased Lordosis/Scoliosis, Hyporeflexia, Duchenne Muscular Dystrophy, Red-Green Color Blindness, Lordosis, Scoliosis, Muscular Atrophy, Muscular Weakness
Locations: Ain Shams University-Medical Genetics, Cairo, Egypt
Ain Shams University, Cairo, Egypt
Ain Shams Univirsity, Cairo, Egypt
Amrita Institute of Medical Sciences & Research Centre, Cochin, Kerala, India
Navi Mumbai Institute of Research In Mental And Neurological Handicap (NIRMAN), Mumbai, India
... and 7 other locations.
The Global FKRP Patient Registry
Status: Recruiting
Last Changed: Jul 02, 2019
First Received: Jun 28, 2019
Disease(s): LGMD2I, LGMDR9, Limb Girdle Muscular Dystrophy, Congenital Muscular Dystrophy, Muscle-Eye-Brain Disease, Walker-Warburg Syndrome, FKRP Gene Mutation
Intervention(s): Patient Registry
Locations: The John Walton Muscular Dystrophy Research Centre, Newcastle upon-Tyne, United Kingdom