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Early Experience With Descemet's Stripping Automated Endothelial Keratoplasty

NCT00744796 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 21

Last updated 2020-12-11

Study results available
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Summary

The purpose of this study is to report the early clinical outcomes in patients undergoing Descemet's Stripping Automated Endothelial Keratoplasty (DSAEK) for corneal edema secondary to corneal endothelial cell dysfunction, and to correlate this clinical data with the latest generation of imaging modalities available for the anterior segment.

Conditions

  • Corneal Edema Secondary to Corneal Endothelial Dystrophy

Interventions

PROCEDURE

DSAEK

Endothelial Keratoplasty

DIAGNOSTIC_TEST

Anterior Segment Optical Coherence Topography (OCT)

Non-contact, high resolution, cross sectional imaging of the anterior segment of the eye.

DIAGNOSTIC_TEST

Best Spectacle Corrected Visual Acuity (BSCVA)

Visual acuity determined using a combination of detecting hand motion, counting fingers displayed and reading Snellen charts at specific distances.

Sponsors & Collaborators

  • University of Texas Southwestern Medical Center

    lead OTHER

Principal Investigators

  • Vinod Mootha, MD · UTSW Medical Center at Dallas

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2006-12-31
Primary Completion
2008-07-31
Completion
2009-07-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00744796 on ClinicalTrials.gov