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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)

Sponsor
University of Texas Southwestern Medical Center (Other)
Overall Status
Withdrawn
CT.gov ID
NCT00344604
Collaborator
(none)
0
Enrollment
1
Location
27
Duration (Months)
0
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Role of psychosocial and quality of life parameters prior to and following LASIK.

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 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

Study Type:
Observational
Actual Enrollment :
0 participants
Time Perspective:
Prospective
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)
Study Start Date :
Mar 1, 2004
Actual Study Completion Date :
Jun 1, 2006

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    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™.

    -

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Texas Southwestern Medical Center at Dallas Dallas Texas United States 75390-8866

    Sponsors and Collaborators

    • University of Texas Southwestern Medical Center

    Investigators

    • Principal Investigator: Shady Awwad, M.D., University of Texas, Southwestern Medical Center at Dallas

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00344604
    Other Study ID Numbers:
    • 032004-028
    First Posted:
    Jun 27, 2006
    Last Update Posted:
    Dec 13, 2018
    Last Verified:
    Dec 1, 2018
    Keywords provided by , ,
    Patients who have undergone routine LASIK as a primary refractive procedure for myopia, hyperopia, or astigmatism.

    Study Results

    No Results Posted as of Dec 13, 2018