WithdrawnNot Applicable

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)

Stopped: PI decided to terminate the study at this time

United States0Started 2004-03

Plain-language summary

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

Who can participate

Age range18 Years – 70 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: All refractive surgery patients with otherwise normal eyes undergoing routine LASIK as a primary refractive procedure for myopia, hyperopia or astigmatism. \- Exclusion Criteria: Patients who elect to perform alternative refractive surgery such as PRK, RK, or Intacts™. \-

Trial details

NCT IDNCT00344604

SponsorUniversity of Texas Southwestern Medical Center

Sponsor typeOTHER

Study typeOBSERVATIONAL

View on ClinicalTrials.gov More Keratomileusis, Laser In Situ trials