An Observational Study of Dry Eye Prior to Laser-Assisted in Situ Keratomileusis (LASIK) Therapy

Study Identifier
MAF-AGN-OPH-DE-015
CT.gov Identifier
NCT01854905
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
    18+ years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    * Attending an ophthalmology consultation for LASIK
    Exclusion Criteria:
    * None

    Protocol Summary

    This is an observational, study of dry eye in patients at the consultation visit prior to LASIK surgery. There is no treatment administered or intervention during the study.

    Study Locations

    Location
    Status
    Location
    Moscow, Russian Federation
    Status
    Not applicable