A Study of Sodium Carboxymethylcellulose for Post Cataract Surgery Dry Eye Symptoms

Study Identifier
CN-CMC-1101
CT.gov Identifier
NCT02028754
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact

844-663-3742 or [email protected]

Study Complete

Study Details

Medical Condition
  • Dry Eye
  • Eye Care - Other
    • Study Drug
  • Sodium Carboxymethylcellulose
  • Levofloxacin
  • Prednisolone
    • Phase
    Phase 4
    Sex
    Female & Male
    Age
    60 - 80 Years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Diagnosis of age-related cataract in the study eye * Scheduled for cataract surgery and lens implant
    Exclusion Criteria:
    * Diagnosis of ocular surface disease or glaucoma * Ocular surgery in the past 3 months * Wearing a corneal contact lens in the study eye

    Protocol Summary

    This study will evaluate the effect of sodium carboxymethylcellulose eye drops in the treatment of dry eye after cataract surgery.

    Study Locations

    Location
    Status
    Location
    Hangzhou, China
    Status
    Not applicable