Clinical Trials on Eye Diseases, Hereditary

Total 630 results

    • NCT00811512
      Completed
      Conditions: Eye Diseases, Hereditary
    • NCT00011817
      Completed
      Conditions: Hereditary Eye Disease
    • NCT00001732
      Completed
      Conditions: Hereditary Eye Disease
    • NCT02946879
      Recruiting
      Conditions: Leber Congenital Amaurosis (LCA); Eye Diseases; Eye Diseases, Hereditary; Retinal Diseases
    • NCT02157077
      Completed
      Conditions: Macular Degeneration; Wet Macular Degeneration; Retinal Degeneration; Retinal Diseases; Eye Diseases
    • NCT04005352
      Recruiting
      Conditions: Age-related Macular Degeneration; Macular Degeneration; Wet Macular Degeneration; Retinal Degeneration; Retinal Diseases; Eye Diseases
    • NCT03954626
      Completed
      Conditions: Age-Related Macular Degeneration; Macular Degeneration; Wet Macular Degeneration; Retinal Degeneration; Retinal Diseases; Eye Diseases
    • NCT02348359
      Terminated
      Conditions: Age-Related Macular Degeneration (AMD); Macular Degeneration; Exudative Age-related Macular Degeneration; AMD; Macular Degeneration, Age-related, 10; Eye Diseases; Retinal Degeneration; Retinal Diseases
    • NCT01399515
      Completed
      Conditions: Retinitis Pigmentosa; Retinal Diseases; Eye Diseases; Eye Disease, Hereditary; Retinal Degeneration
    • NCT01878032
      Completed
      Conditions: Healthy Volunteer; Retinal Disease; Inherited Retinal Degeneration
    • NCT01736293
      Active, not recruiting
      Conditions: Retinal Degeneration; ABCA4-Related Retinopathies
    • NCT00877032
      Completed
      Conditions: Age-Related Maculopathy; Age-Related Maculopathies; Eye Diseases; Retinal Degeneration; Macular Degeneration
    • NCT04545736
      Recruiting
      Conditions: ABCA4 Retinopathy; Stargardt Disease; Retinal Dystrophy; Retinal Degeneration
    • NCT03592017
      Unknown status
      Conditions: Retinal Disease; Retinal Degeneration; Retinal Dystrophies
    • NCT03872479
      Recruiting
      Conditions: Blindness; Leber Congenital Amaurosis 10; Vision Disorders; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Retinal Disease; Retinal Degeneration
    • NCT04123626
      Recruiting
      Conditions: Autosomal Dominant Retinitis Pigmentosa; Eye Diseases; Eye Diseases, Hereditary; Retinal Dystrophies; Retinal Disease; Retinitis; Vision Tunnel; Vision Disorders
    • NCT03396042
      Recruiting
      Conditions: Blindness; Leber Congenital Amaurosis 10; Vision Disorders; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Retinal Disease; Retinal Degeneration
    • NCT02203682
      Unknown status
      Conditions: Graves Ophthalmopathy; Graves Disease; Eye Diseases; Thyroid Diseases; Endocrine System Diseases; Eye Diseases, Hereditary; Hyperthyroidism; Autoimmune Diseases; Immune System Diseases
    • NCT03780257
      Recruiting
      Conditions: Retinitis Pigmentosa; Usher Syndrome Type 2; Deaf Blind; Retinal Disease; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Vision Disorders
    • NCT03913143
      Recruiting
      Conditions: Leber Congenital Amaurosis 10; Blindness; Leber Congenital Amaurosis; Vision Disorders; Sensation Disorders; Neurologic Manifestations; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Retinal Disease
    • NCT03913130
      Active, not recruiting
      Conditions: Leber Congenital Amaurosis 10; Blindness; Leber Congenital Amaurosis; Vision Disorders; Sensation Disorders; Neurologic Manifestations; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Retinal Disease
    • NCT01727973
      Completed
      Conditions: Graves Ophthalmopathy; Graves Disease; Eye Diseases; Thyroid Diseases; Endocrine System Diseases; Eye Diseases, Hereditary; Hyperthyroidism; Autoimmune Diseases; Immune System Diseases
    • NCT01432847
      Recruiting
      Conditions: Retinal Disease; AMD; Retinal Degeneration; Retinitis Pigmentosa
    • NCT02435940
      Recruiting
      Conditions: 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
    • NCT00357435
      Completed
      Conditions: Corneal Dystrophies, Hereditary; Corneal Disease