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)

Keratomileusis, Laser In Situ Clinical Trial

Official title:
The Role of Psychosocial and Other Quality of Life Parameters in Evaluating Functional Changes Prior to and Following Laser In-situ Keratomileusis (LASIK)

Status Withdrawn

Clinical Trial Summary

To evaluate the changes in quality of life parameters after LASIK surgery.

Clinical Trial 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 visit and at the 1-month and 3-month post-operative visits. Additional questionnaires will be administered to demonstrate the validity of the new questionnaire. The approximate time the patient will be required to spend in clinic will be approximately 45 minutes at each of the three visits. ;

Study Design

Related Conditions & MeSH terms

Keratomileusis, Laser In Situ

Clinical Trial Details

NCT number	NCT00344604
Study type	Observational
Source	University of Texas Southwestern Medical Center
Contact
Status	Withdrawn
Phase
Start date	March 2004
Completion date	June 2006

View Details

See also
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