Prospective Comparison of Cirrus Versus Stratus Ocular Coherence Tomography for Different Retinal Pathology.

Sponsor
University of Chicago (Other)
Overall Status
Completed
CT.gov ID
NCT00731458
Collaborator
Research to Prevent Blindness (Other)
60
6

Study Details

Study Description

Brief Summary

Ocular Coherence Tomography (OCT) is a non-invasive ophthalmologic test that uses reflected, unheated, non-concentrated visible light in order to scan and provide a 2-dimensional topographic analysis of the retina and optic nerve. It has wide diagnostic utility especially in patients with clinically significant macular edema, glaucoma, and other retinal eye diseases. At the University of Chicago, we have utilized the Stratus brand OCT (Carl Zeiss Inc) for the past 5 years. Recently we have acquired a beta version of the company's new model, the Cirrus HD-OCT (Carl Zeiss Inc.) which features improved resolution, shorter scanning time and a more user-friendly interface. The purpose of this study is to compare findings between the two models in patients with different common and uncommon eye diseases, including diabetic macular edema, glaucoma and age-related macular degeneration. We hypothesis that the Cirrus OCT is able to accurately quantify eye pathology compared to Stratus OCT.

Condition or Disease Intervention/Treatment Phase
  • Device: Optical coherance tomography ( Cirrus; Stratus)
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Prospective Comparison of Cirrus and Stratus Optical Coherence Tomography for Quantifying Retinal Thickness
Study Start Date :
May 1, 2007
Actual Primary Completion Date :
Nov 1, 2007
Actual Study Completion Date :
Nov 1, 2007

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Any eye pathology that may cause macular edema.
    Exclusion Criteria:
    • Vitreous media opacities including dense cataracts, vitreous hemorrhage, and corneal opacities

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University of Chicago
    • Research to Prevent Blindness

    Investigators

    • Principal Investigator: Seenu Hariprasad, M.D., University of Chicago

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    University of Chicago
    ClinicalTrials.gov Identifier:
    NCT00731458
    Other Study ID Numbers:
    • 15606B
    First Posted:
    Aug 11, 2008
    Last Update Posted:
    Sep 5, 2013
    Last Verified:
    Sep 1, 2013
    Keywords provided by University of Chicago

    Study Results

    No Results Posted as of Sep 5, 2013