Efficacy Study of Cyclosporine Ophthalmic Emulsion in Patients With Dry Eye Disease

Study Identifier
R.E.S.T.O.R.E.
CT.gov Identifier
NCT00717418
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
  • cyclosporine ophthalmic emulsion 0.05%, artificial tears
    • Phase
    N/A
    Sex
    Female & Male
    Age
    N/A
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    Inclusion Criteria: * Diagnosis of dry eye disease * Currently using artificial tears daily * Male or female of legal age of consent * Normal lid position and closure Exclusion Criteria * Patients currently using cyclosporine ophthalmic emulsion 0.05% * Participation in other investigational drug or device study * Any current or previous topical ophthalmic or oral cyclosporine use within the last three years

    Protocol Summary

    This study will evaluate the efficacy of cyclosporine ophthalmic solution vs. other non-prescription treatments in patients with dry eye disease. Patient and physician assessments completed at baseline, at each follow-up visit (follow-up visits are variable as per physician discretion) and at final follow-up visit.

    Study Locations

    Location
    Status
    Location
    Wilson, North Carolina, United States
    Status
    Not applicable