Evaluation of vision quality after LASIK, SMILE, and PRK surgery in physicians

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

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 it's running

• 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

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.