Study to Compare the Efficacy and Safety of Two Non-Preserved Artificial Tears for the Treatment of Dry Eye Signs and Symptoms

Study Identifier
MA-OPT-09-002
CT.gov Identifier
NCT00938704
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
  • carboxymethylcellulose 0.5% +glycerin 0.9%
  • sodium hyaluronate 0.18%
    • Phase
    Phase 4
    Sex
    Female & Male
    Age
    18+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Current use of an artificial tear product at least 2 times per day (e.g. for relief of dry eye symptoms of dryness). * Be likely to complete the entire course of study and to comply with appropriate instructions
    Exclusion Criteria:
    * Have undergone refractive surgery (e.g., cataract surgery, PRK, LASIK, or any surgery involving a limbal or corneal incision) within the last 12 months. * Have uncontrolled systemic disease * Are currently using, or have used within 14 days of study enrollment, any ocular medications other than artificial tears * Have anticipated contact lens wear during the study * Have an active ocular infection

    Protocol Summary

    To compare the efficacy and safety of two non-preserved artificial tears, (carboxymethylcellulose 0.5%, + glycerin 0.9% vs. sodium hyaluronate 0.18%) eye drops for the treatment of the signs and symptoms of dry eye disease.

    Study Locations

    Location
    Status
    Location
    Ulm, Germany
    Status
    Not applicable