Example: Heart Attack
Clinical Trials on Ophthalmoplegia
Total 118 results
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NCT03269682RecruitingConditions: Ophthalmoplegia
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NCT03135574RecruitingConditions: Ophthalmoplegia
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NCT02161848CompletedConditions: Chronic Progressive External Ophthalmoplegia
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NCT04436198RecruitingConditions: Cataract; Ophthalmoplegia; Ophthalmologic Complication
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NCT02391961CompletedConditions: Multiple Sclerosis; Internuclear Ophthalmoplegia; Fatigue
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NCT03432871RecruitingConditions: 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)
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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 OphthalmoplegiaNCT00753831CompletedConditions: Ptosis, EyelidNCT02385565CompletedConditions: 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 SyndromeNCT03059420RecruitingConditions: Congenital Fibrosis of Extraocular Muscles; Duane Retraction Syndrome; Duane Radial Ray Syndrome; Mobius Syndrome; Brown Syndrome; Marcus Gunn Syndrome; Strabismus Congenital; Horizontal Gaze Palsy; Horizontal Gaze Palsy With Progressive Scoliosis; Facial Palsy; Facial Paresis, Hereditary, Congenital; Third Nerve Palsy; Fourth Nerve Palsy; Sixth Nerve Palsy; Synkinesis; Ocular Motility Disorders; Levator-Medial Rectus Synkinesis; Athabaskan Brainstem Dysgenesis; Tongue Paralysis; Ninth Nerve Disorder; Fifth Nerve Palsy; Seventh Nerve Palsy; Eleventh Nerve Disorder; Twelfth Nerve Disorder; Vagus Nerve Paralysis; Moebius SequenceNCT04691635Not yet recruitingConditions: Progressive Supranuclear PalsyNCT04253132Not yet recruitingConditions: Progressive Supranuclear PalsyNCT04786158CompletedConditions: Progressive Supranuclear Palsy; Corticobasal DegenerationNCT04753320Not yet recruitingConditions: Progressive Supranuclear PalsyNCT04734379RecruitingConditions: Progressive Supranuclear Palsy; Corticobasal SyndromeNCT04715750RecruitingConditions: Alzheimer Disease; Progressive Supranuclear PalsyNCT04715399RecruitingConditions: Frontotemporal Degeneration(FTD); Primary Progressive Aphasia(PPA); Familial Frontotemporal Lobar Degeneration (fFTLD); Amyotrophic Lateral Sclerosis(ALS); Lewy Body Disease(LBD); Progressive Supranuclear Palsy(PSP); Corticobasal Syndrome(CBS); Posterior Cortical Atrophy(PCA); Alzheimer's Disease(AD)NCT04706234RecruitingConditions: Multiple System Atrophy; Parkinson Disease; Progressive Supranuclear PalsyNCT04658199Enrolling by invitationConditions: Progressive Supranuclear PalsyNCT04655079Not yet recruitingConditions: Progressive Supranuclear Palsy; Motor and Cognitive SymptomsNCT04608604RecruitingConditions: Multiple System Atrophy, Parkinson Variant (Disorder); Parkinson Disease; Progressive Supranuclear PalsyNCT04541836RecruitingConditions: Progressive Supranuclear Palsy