Status:
WITHDRAWN
The Role of Psychosocial and Other Quality of Life Parameters in Evaluating Functional Changes Prior to and Following Laser In-situ Keratomileusis (LASIK)Changes Laser In-situ Keratomileusis (LASIK)
Lead Sponsor:
University of Texas Southwestern Medical Center
Conditions:
Keratomileusis, Laser In Situ
Eligibility:
All Genders
18-70 years
Brief Summary
To evaluate the changes in quality of life parameters after LASIK surgery.
Detailed Description
Our purpose is to evaluate the changes in quality of life parameters after LASIK surgery. We intend to create a questionnaire to delineate the changes that occur in LASIK patients at the pre-operative...
Eligibility Criteria
Inclusion
- All refractive surgery patients with otherwise normal eyes undergoing routine LASIK as a primary refractive procedure for myopia, hyperopia or astigmatism.
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Exclusion
- Patients who elect to perform alternative refractive surgery such as PRK, RK, or Intacts™.
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Key Trial Info
Start Date :
March 1 2004
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
June 1 2006
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT00344604
Start Date
March 1 2004
End Date
June 1 2006
Last Update
December 13 2018
Active Locations (1)
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1
University of Texas Southwestern Medical Center at Dallas
Dallas, Texas, United States, 75390-8866