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  • Conditions:   Usher Syndrome;   Retinitis Pigmentosa
    Intervention:   Genetic: SAR421869
    Sponsor:   Sanofi
    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
    Intervention:  
    Sponsor:   Foundation Fighting Blindness
    Recruiting

  • Conditions:   Retinitis Pigmentosa;   Usher Syndrome Type 2;   Deaf Blind;   Retinal Disease;   Eye Diseases;   Eye Diseases, Hereditary;   Eye Disorders Congenital;   Vision Disorders
    Interventions:   Drug: QR-421a;   Other: Sham-procedure
    Sponsor:   ProQR Therapeutics
    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
    Interventions:   Procedure: Arm 1;   Procedure: Arm 2;   Procedure: Arm 3
    Sponsor:   MD Stem Cells
    Recruiting

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