Clinical Trials on Usher Syndromes

Total 19 results





    • NCT04355689
      Recruiting
      Conditions: Usher Syndromes
    • NCT02065011
      Active, not recruiting
      Conditions: Usher's Syndrome
    • NCT03814499
      Recruiting
      Conditions: Usher Syndrome, Type 1B
    • NCT01505062
      Terminated
      Conditions: Usher Syndrome; Retinitis Pigmentosa
    • NCT01954953
      Unknown status
      Conditions: Usher Syndrome
    • NCT03319524
      Completed
      Conditions: Usher Syndrome; Congenital Deafness; Retinitis Pigmentosa
    • NCT00004345
      Terminated
      Conditions: Usher Syndrome; Retinitis Pigmentosa
    • NCT00016471
      Completed
      Conditions: Usher Syndrome; Retinitis Pigmentosa; Congenital Hearing Impairment
    • NCT00106743
      Completed
      Conditions: Retinitis Pigmentosa Syndromic; Congenital Deafness; Usher Syndrome; Retinitis Pigmentosa and Deafness; Retinitis Pigmentosa
    • NCT00001347
      Completed
      Conditions: Retinitis Pigmentosa
    • NCT03901391
      Enrolling by invitation
      Conditions: Retinitis Pigmentosa; Usher Syndromes
    • NCT01530659
      Active, not recruiting
      Conditions: Retinitis Pigmentosa; Usher Syndrome Type 2; Usher Syndrome Type 3
    • NCT03146078
      Active, not recruiting
      Conditions: Usher Syndrome, Type 2A; Retinitis Pigmentosa 39
    • NCT03990727
      Recruiting
      Conditions: Retinitis Pigmentosa; Cone Dystrophy; Usher Syndromes; Retina; Dystrophy
    • 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
    • NCT03780257
      Recruiting
      Conditions: Retinitis Pigmentosa; Usher Syndrome Type 2; Deaf Blind; Retinal Disease; Eye Diseases; Eye Diseases, Hereditary; Eye Disorders Congenital; Vision Disorders
    • NCT00341874
      Recruiting
      Conditions: Hearing Disorder
    • NCT03011541
      Recruiting
      Conditions: Retinal Disease; Age-Related Macular Degeneration; Retinitis Pigmentosa; Stargardt Disease; Optic Neuropathy; Nonarteritic Ischemic Optic Neuropathy; Optic Atrophy; Optic Nerve Disease; Glaucoma; Leber Hereditary Optic Neuropathy; Blindness; Vision Loss Night; Vision Loss Partial; Vision, Low; Retinopathy; Maculopathy; Macular Degeneration; Retina Atrophy
    • NCT00231010
      Completed
      Conditions: Retinal Degeneration; Retinitis Pigmentosa