Tear Collection in Adult Volunteers

Study Identifier
195263-008
CT.gov Identifier
NCT01969162
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
  • Healthy Volunteer
    • Study Drug
    N/A
    Phase
    N/A
    Sex
    Female & Male
    Age
    18 - 40 Years
    Inclusion and Exclusion Criteria
    Inclusion Criteria:
    -Adult volunteers without ocular disease.
    Exclusion Criteria:
    * Systemic medications that could affect eye health taken within 1 month of enrollment * Eye infection or inflammation in either eye 3 months prior to screening * History of herpes in either eye * Diagnosis of dry eye or meibomian gland dysfunction * Diagnosis of glaucoma * Allergic conjunctivitis * Use of rigid contact lenses within 1 year of screening * Use of soft contact lenses within 1 week of enrollment.

    Protocol Summary

    This exploratory study will collect tear samples from adult volunteers for determining and quantifying tear composition profiles. No investigational drug will be administered in this study.

    Study Locations

    Location
    Status
    Location
    Randwick, New South Wales, Australia
    Status
    Not applicable