Clinical Trials on Color Vision Defects

Total 17 results





    • NCT04124185
      Recruiting
      Conditions: Achromatopsia
    • NCT04060238
      Completed
      Conditions: Color Blindness, Red; Reaction Time
    • NCT04048499
      Completed
      Conditions: CAD Test; Children's Vision; Colour Assessment; Colour Vision; Turkey
    • NCT04041232
      Not yet recruiting
      Conditions: ACHROMATOPSIA 7; Achromatopsia
    • NCT04021914
      Suspended
      Conditions: Color Vision Defects
    • NCT03758404
      Recruiting
      Conditions: Achromatopsia
    • NCT03278873
      Recruiting
      Conditions: Achromatopsia
    • NCT03001310
      Completed
      Conditions: Achromatopsia
    • NCT02994030
      Recruiting
      Conditions: Increased Lordosis/Scoliosis; Hyporeflexia; Duchenne Muscular Dystrophy; Red-Green Color Blindness; Lordosis; Scoliosis; Muscular Atrophy; Muscular Weakness
    • NCT02935517
      Recruiting
      Conditions: Achromatopsia
    • NCT02909985
      Completed
      Conditions: Age Related Macular Degeneration; Retinitis Pigmentosa; Congenital Stationary Night Blindness; Colorblindness
    • NCT02610582
      Active, not recruiting
      Conditions: Achromatopsia
    • NCT02599922
      Recruiting
      Conditions: Achromatopsia
    • 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
    • NCT01927536
      Completed
      Conditions: Color Blindness, Acquired
    • NCT01846052
      Completed
      Conditions: Achromatopsia
    • NCT01648452
      Completed
      Conditions: Eye Disease; Achromatopsia