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Mitochondrial disorders

Mitochondrial genetic disordersMitochondrial diseases
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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 151-160 of 243 results.
Transcorneal Electrical Stimulation Therapy for Retinal Disease
Status: Completed
Last Changed: May 04, 2012
First Received: Dec 08, 2008
Disease(s): Retinitis Pigmentosa, Macula Off, Primary Open Angle Glaucoma, Hereditary Macular Degeneration, Treated Retina Detachment, Retinal Artery Occlusion, Retinal Vein Occlusion, Non-Arthritic-Anterior-Ischemic Optic-Neuropathy, Hereditary Autosomal Dominant Optic Atrophy, Dry Age Related Macular Degeneration, Ischemic Macula Edema
Intervention(s): Transcorneal Electrical Stimulation, DTL-electrode attached without energy
Efficacy Study of Gene Therapy for The Treatment of Acute LHON Onset Within Three Months
Status: Active, not recruiting
Last Changed: Jul 29, 2020
First Received: Feb 09, 2018
Disease(s): Acute LHON, Onset Within Three Months, Onset Between 3 to 6 Months, Onset Between 6 to 12 Months, Onset Between 12 to 24 Months, Onset Between 24 to 60 Months, Onset Over 60 Months
Intervention(s): rAAV2-ND4
Locations: Department of Ophthalmology ,Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China
Neurology Measures in FA Children
Status: Recruiting
Last Changed: Apr 29, 2020
First Received: Feb 01, 2018
Disease(s): Friedreich Ataxia
Locations: University of California, Los Angeles, Los Angeles, California, United States
University of Florida, Gainesville, Florida, United States
Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States
Rehabilitative Trial With Cerebello-Spinal tDCS in Neurodegenerative Ataxia
Status: Completed
Last Changed: Mar 03, 2020
First Received: Apr 19, 2017
Disease(s): Ataxia, Cerebellar, Cerebellar Ataxia, Spinocerebellar Ataxias, Ataxia, Spinocerebellar, Spinocerebellar Ataxia Type 1, Spinocerebellar Ataxia Type 2, Spinocerebellar Ataxia 3, Spinocerebellar Degenerations, Friedreich Ataxia, Ataxia With Oculomotor Apraxia, Multiple System Atrophy
Intervention(s): Anodal cerebellar and cathodal spinal tDCS, Sham cerebellar and sham spinal tDCS
Locations: AO Spedali Civili, Brescia, BS, Italy
L-arginine Therapy on Endothelium-dependent Vasodilation & Mitochondrial Metabolism in MELAS Syndrome
Status: Completed
Last Changed: Dec 17, 2013
First Received: May 22, 2012
Disease(s): MELAS Syndrome
Intervention(s): L-Arginine
Locations: The Hospital for Sick Children, Toronto, Ontario, Canada
Efficacy, Tolerability, and Pharmacokinetics of Multiple Doses of Oral TAK-831 in Adults With Friedreich Ataxia
Status: Completed
Last Changed: Dec 19, 2019
First Received: Jul 11, 2017
Disease(s): Friedreich Ataxia
Intervention(s): TAK-831, TAK-831 Placebo
Locations: UCLA Ataxia Center, Los Angeles, California, United States
University of Florida Center for Movement Disorders, Gainesville, Florida, United States
USF College of Medicine, Tampa, Florida, United States
University of Iowa Children's Hospital, Iowa City, Iowa, United States
Ohio State University Wexner Medical Center, Columbus, Ohio, United States
... and 2 other locations.
TCA Cycle in the Dentate in Friedreich's Ataxia
Status: Enrolling by invitation
Last Changed: Sep 04, 2020
First Received: Apr 21, 2017
Disease(s): Friedreich Ataxia
Intervention(s): MR
Locations: CMRR, Minneapolis, Minnesota, United States
Trial of Cyclosporine in the Acute Phase of Leber Hereditary Optic Neuropathy
Status: Unknown status
Last Changed: Jun 27, 2014
First Received: Jun 27, 2014
Disease(s): Leber Hereditary Optic Neuropathy
Intervention(s): cyclosporine
Locations: Centre Hospitalier Universitaire, Angers, France
Emergency Administration of EPI-743 to a Single Patient With Leber's Hereditary Optic Neuropathy [LHON]
Status: No longer available
Last Changed: Nov 25, 2014
First Received: Nov 25, 2014
Disease(s): Leber's Hereditary Optic Neuropathy
Intervention(s): EPI-743
Locations: Doheny Eye Institute / UCLA, Los Angeles, California, United States
Short-Term Outcome of N-Carbamylglutamate in the Treatment of Acute Hyperammonemia
Status: Active, not recruiting
Last Changed: Jun 11, 2019
First Received: May 16, 2012
Disease(s): Propionic Acidemia, Type I and/or Type II, Methylmalonic Acidemia, Carbamoyl-Phosphate Synthase I Deficiency Disease, Ornithine Carbamoyltransferase Deficiency
Intervention(s): Carbaglu, Placebo, Standard of Care Treatment
Locations: University of California Los Angeles, Los Angeles, California, United States
Lucile Packard Children's Hospital at Stanford, Palo Alto, California, United States
The Children's Hospital of Colorado, Aurora, Colorado, United States
Children's National Medical Center, Washington, District of Columbia, United States
Children's Hospital Boston, Boston, Massachusetts, United States
... and 5 other locations.