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Clinical Trials on Leber Congenital Amaurosis
Total 28 results
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NCT02970266CompletedConditions: Leber Congenital Amaurosis
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NCT03140969CompletedConditions: Leber's Congenital Amaurosis
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NCT03920007RecruitingConditions: Leber's Congenital Amaurosis
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NCT02714816RecruitingNatural History Study of Patients With Leber Congenital Amaurosis Associated With Mutations in RPE65Conditions: Leber Congenital Amaurosis
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NCT00516477CompletedConditions: Leber Congenital Amaurosis
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NCT00749957CompletedConditions: Leber Congenital Amaurosis
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NCT01208389Active, not recruitingConditions: Leber Congenital Amaurosis
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NCT02781480CompletedConditions: Leber Congenital Amaurosis
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NCT00999609Active, not recruitingConditions: Inherited Retinal Dystrophy Due to RPE65 Mutations; Leber Congenital Amaurosis
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NCT00821340CompletedConditions: Leber Congenital Amaurosis
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NCT01521793CompletedConditions: LCA (Leber Congenital Amaurosis); RP (Retinitis Pigmentosa)
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NCT01014052CompletedConditions: LCA (Leber Congenital Amaurosis); RP (Retinitis Pigmentosa)
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NCT03566147Unknown statusConditions: Leber Congenital Amaurosis, Retinitis Pigmentosa
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NCT01496040CompletedConditions: Leber Congenital Amaurosis
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NCT04525261RecruitingConditions: Leber Congenital Amaurosis 2; Retinitis Pigmentosa 20
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NCT00643747CompletedConditions: Retinal Degeneration
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NCT02946879RecruitingConditions: Leber Congenital Amaurosis (LCA); Eye Diseases; Eye Diseases, Hereditary; Retinal Diseases
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NCT02575430CompletedConditions: Leber Congenital Amaurosis (LCA); Retinitis Pigmentosa (RP)
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NCT00481546Active, not recruitingConditions: Amaurosis of Leber; Retinal Diseases
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NCT03913130Active, not recruitingConditions: Leber Congenital Amaurosis 10; Blindness; Leber Congenital Amaurosis; Vision Disorders; Sensation Disorders; Neurologic Manifestations; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Retinal Disease
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NCT03913143Active, not recruitingConditions: Leber Congenital Amaurosis 10; Blindness; Leber Congenital Amaurosis; Vision Disorders; Sensation Disorders; Neurologic Manifestations; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Retinal Disease
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NCT03872479RecruitingConditions: Blindness; Leber Congenital Amaurosis 10; Vision Disorders; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Retinal Disease; Retinal Degeneration
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NCT03396042RecruitingConditions: Blindness; Leber Congenital Amaurosis 10; Vision Disorders; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Retinal Disease; Retinal Degeneration
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NCT03602820Active, not recruitingConditions: Inherited Retinal Dystrophy Due to RPE65 Mutations
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NCT02435940RecruitingConditions: 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 Syndrome