Example: Heart Attack
Clinical Trials on Ophthalmoplegia, Chronic Progressive External
Total 9 results
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NCT02161848CompletedConditions: Chronic Progressive External Ophthalmoplegia
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NCT04604548Not yet recruitingConditions: Mitochondrial Diseases; Mitochondrial DNA tRNALeu(UUR) m.3243ANCT04678115Not yet recruitingConditions: Blepharoptosis; Ptosis, Eyelid; Myasthenia Gravis; Stroke; Traumatic Brain Injury; Chronic Progressive External OphthalmoplegiaNCT03432871RecruitingConditions: 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)NCT02385565CompletedConditions: Mitochondrial Cytopathies DisordersNCT02375438CompletedConditions: Mitochondrial Diseases; Mitochondrial Myopathies; Mitochondrial CytopathiesNCT02435940RecruitingConditions: Eye Diseases Hereditary; Retinal Disease; Achromatopsia; Bardet-Biedl Syndrome; Bassen-Kornzweig Syndrome; Batten Disease; Best Disease; Choroidal Dystrophy; Choroideremia; Cone Dystrophy; Cone-Rod Dystrophy; Congenital Stationary Night Blindness; Enhanced S-Cone Syndrome; Fundus Albipunctatus; Goldmann-Favre Syndrome; Gyrate Atrophy; Juvenile Macular Degeneration; Kearns-Sayre Syndrome; Leber Congenital Amaurosis; Refsum Syndrome; Retinitis Pigmentosa; Retinitis Punctata Albescens; Retinoschisis; Rod-Cone Dystrophy; Rod Dystrophy; Rod Monochromacy; Stargardt Disease; Usher SyndromeNCT03888716RecruitingConditions: Mitochondrial Diseases; Mitochondrial Respiratory Chain Deficiencies; MELAS Syndrome; Mitochondrial MyopathiesNCT01694940RecruitingConditions: Mitochondrial Disorders; Mitochondrial Genetic Disorders; Mitochondrial Diseases; Disorder of Mitochondrial Respiratory Chain Complexes; Deletion and Duplication of Mitochondrial DNA