CXCL9, CXCL10, CXCL11, and CXCR3 in Dry Eye Syndrome

Sponsor
Chonnam National University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT00991679
Collaborator
(none)
48
1
10
4.8

Study Details

Study Description

Brief Summary

The aim of this study is to investigate the expression of CXCL9, CXCL10, CXCL11, and CXCR3 in the tear film and ocular surface of patients with dry eye syndrome.

Thirty-three patients with dry eye (16 Sjögren's syndrome and 17 non-Sjögren's syndrome patients) and 15 control subjects were recruited. The concentrations of CXCL9, CXCL10, and CXCL11 in tears were measured using enzyme-linked immunosorbent assay. The correlation between chemokine levels and tear film and ocular surface parameters was analyzed. Expression of CXCL9, CXCL10, CXCL11, and CXCR3 in the conjunctiva was evaluated using immunohistochemistry. Flow cytometry was performed to count CXCR3+ cells and CXCR3+CD4+ cells in the conjunctiva.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    48 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Expression of CXCL9, CXCL10, CXCL11, and CXCR3 in the Tear Film and Ocular Surface of Patients With Dry Eye Syndrome
    Study Start Date :
    Feb 1, 2008
    Actual Primary Completion Date :
    Oct 1, 2008
    Actual Study Completion Date :
    Dec 1, 2008

    Arms and Interventions

    Arm Intervention/Treatment
    Normal control subjects

    Normal control subjects who did not show the clinical symptom and findings of dry eye syndrome.

    dry eye patients

    Patients with dry eye syndrome who had symptoms of dry eye for more than 3 months, low tear film break up time (BUT, ≤7 sec), low Schirmer test (<10 mm), low tear clearance rate (<8X), and positive fluorescein or rose bengal vital staining (≥3) and were not treated with anti-inflammatory agents such as topical cyclosporine or steroids were included in the study.

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      24 Years to 77 Years
      Sexes Eligible for Study:
      All
      Accepts Healthy Volunteers:
      Yes
      Inclusion Criteria:
      • clinical diagnosis of dry eye syndrome
      Exclusion Criteria:
      • active ocular infection or inflammation not associated with dry eye

      • drug toxicity

      • contact lens wear

      • ocular allergy

      • ocular surgery within the last 3 months

      • lid or lash abnormalities

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 Chonnam National University Hospital Gwangju Chonnam Korea, Republic of 501-757

      Sponsors and Collaborators

      • Chonnam National University Hospital

      Investigators

      • Study Director: Kyung-Chul Yoon, MD, PhD, Department of Ophthalmology, Chonnam National University Medical School and Hospital, Gwangju, South Korea

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      None provided.
      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00991679
      Other Study ID Numbers:
      • I-2007-12-111
      First Posted:
      Oct 8, 2009
      Last Update Posted:
      Oct 8, 2009
      Last Verified:
      Oct 1, 2009

      Study Results

      No Results Posted as of Oct 8, 2009