Evaluation of vision quality after LASIK, SMILE, and PRK surgery in physicians
An Evaluation of Quality of Vision and Quality of Life With LASIK, SMILE and PRK Surgery in Physicians
This study is testing how LASIK, SMILE, and PRK eye surgeries affect the vision quality and overall life satisfaction of doctors.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 700 (estimated) |
| Ages | 21 Years to 62 Years |
| Sex | All |
| Sponsor | Stanford University Academic / other |
| Locations | 1 site (Palo Alto, California) |
| Trial ID | NCT02576483 on ClinicalTrials.gov |
What this trial studies
This study evaluates the self-reported quality of vision and quality of life in physicians who undergo LASIK, SMILE, or PRK eye surgeries. Participants will first undergo a comprehensive eye examination to determine their eligibility for the procedures. If deemed appropriate, they will complete a Quality of Vision (QoV) Questionnaire before and after the surgeries at specified follow-up intervals. The study aims to gather data on the outcomes of these refractive surgeries specifically within the physician population.
Who should consider this trial
Good fit: Ideal candidates for this study are physicians or medical students aged 21 and older who have not previously undergone refractive surgery.
Not a fit: Patients with excessively thin corneas or those with specific eye disorders like keratoconus may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the effectiveness of refractive surgeries in improving vision quality for physicians.
How similar studies have performed: Other studies have shown positive outcomes with LASIK, SMILE, and PRK surgeries, indicating that this approach is supported by existing evidence.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion criteria. * 21 years or older. * A physician or medical student. * Have the ability to give informed consent. * Speak and read English fluently. * Have not previously had any form of refractive surgery, including prior LASIK or cataract surgery. * May benefit from increased spectacle independence. * Have been determined to be a good candidate for the LASIK, SMILE or PRK procedure based on the investigator's assessment of medical and ophthalmic health, general cognitive function, and physical and social limitations. * Have a treatment target of bilateral emmetropia. * Express willingness and potential ability to return for all follow-up examinations through the 12-month follow-up exam under the care of the treating investigator. * Are not enrolled in any other research study. Exclusion criteria. * Subjects under the age of 21. * Patients with excessively thin corneas. * Patients with topographic evidence of keratoconus. * Patients with ectatic eye disorders. * Patients with autoimmune diseases. * Patients who are pregnant or nursing.
Where this trial is running
Palo Alto, California
- Byers Eye Institute at Stanford — Palo Alto, California, United States (Recruiting)
Study contacts
- Principal investigator: Edward E. Manche, MD — Stanford University
- Study coordinator: Linda Schwartz
- Phone: 650 498-7020
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.