A Study to Determine the Prevalence of Inflammatory Dry Eye Disease in Patients Prior to Cataract Removal

Study Identifier
GMA-RES-012-001
CT.gov Identifier
NCT01882413
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
    • Study Drug
    N/A
    Phase
    N/A
    Sex
    Female & Male
    Age
    50+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Scheduled to undergo cataract removal surgery
    Exclusion Criteria:
    * Current use of eye drops or oral medications for allergic conjunctivitis * Serious ocular injury, intraocular surgery, or refractive surgery within 6 months in the study eye * Use of a contact lens within 4 weeks

    Protocol Summary

    This study will evaluate the prevalence of inflammatory dry eye disease in patients prior to cataract surgery. No treatment is administered in this study.

    Study Locations

    Location
    Status
    Location
    Brandon, Manitoba, Canada
    Status
    Not applicable
    Location
    Halifax, Nova Scotia, Canada
    Status
    Not applicable
    Location
    Barrie, Ontario, Canada
    Status
    Not applicable
    Location
    Ottawa, Ontario, Canada
    Status
    Not applicable
    Location
    Toronto, Ontario, Canada
    Status
    Not applicable
    Location
    Boisbriand, Quebec, Canada
    Status
    Not applicable