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Prospective Comparison of Cirrus Versus Stratus Ocular Coherence Tomography for Different Retinal Pathology.
This study has been completed.
Sponsors and Collaborators: University of Chicago
Research to Prevent Blindness
Information provided by: University of Chicago
ClinicalTrials.gov Identifier: NCT00731458
  Purpose

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 Intervention
Retinal Pathology
Device: Optical coherance tomography ( Cirrus; Stratus)

U.S. FDA Resources
Study Type: Interventional
Study Design: Health Services Research, Open Label, Uncontrolled, Single Group Assignment
Official Title: Prospective Comparison of Cirrus and Stratus Optical Coherence Tomography for Quantifying Retinal Thickness

Further study details as provided by University of Chicago:

Enrollment: 60
Study Start Date: May 2007
Study Completion Date: November 2007
Primary Completion Date: November 2007 (Final data collection date for primary outcome measure)
Intervention Details:
    Device: Optical coherance tomography ( Cirrus; Stratus)
    Non-contact retinal thickness analyzer
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

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
Please refer to this study by its ClinicalTrials.gov identifier: NCT00731458

Sponsors and Collaborators
University of Chicago
Research to Prevent Blindness
Investigators
Principal Investigator: Seenu Hariprasad, M.D. University of Chicago
  More Information

Publications:
Responsible Party: University of Chicago ( Seenu M Hariprasad )
Study ID Numbers: 15606B
Study First Received: August 6, 2008
Last Updated: August 8, 2008
ClinicalTrials.gov Identifier: NCT00731458  
Health Authority: United States: Institutional Review Board

Keywords provided by University of Chicago:
OCT;
Cirrus;
Stratus;
macular thickness

ClinicalTrials.gov processed this record on January 16, 2009