An Evaluation of LASIK, SMILE and PRK Surgery in Physicians
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age21-62
SponsorStanford University
About this trial
The principle investigator is evaluating self-reported quality of vision and quality of life in physicians undergoing LASIK, SMILE and PRK surgery.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
21 years or older.
A physician or medical student.
Have the ability to give informed consent.
Speak and read English fluently.
Disqualifiers
Subjects under the age of 21.
Patients with excessively thin corneas.
Patients with topographic evidence of keratoconus.
Patients with ectatic eye disorders.
Trial population
Physicians with refractive errors
Trial design
Design model
Cohort
Time perspective
Prospective
Treatments tested in this trial
Questionnaire (QoV questionnaire)
BehavioralQuality of vision and quality of life questionnaire
Treatment groups
No treatment groups listed
Trial outcomes
Primary outcomes
1
Self-reported quality of vision and quality of life questionnaire
Time frame
Twleve monthsSecondary outcomes
1
Predictability (Percentage of eyes within 0.25, +/- 0.50 and +/- 1.00 diopters of the intended correction
Time frame
Preoperatively, one, three, six and twelve months2
Changes in CDVA (Corrected distance visual acuity)
Time frame
Preoperatively, one, three, six and twelve months3
Changes in low contrast acuity (5% and 25% contrast acuity)
Time frame
Preoperatively, one, three, six and twelve months4
Self-reported quality of life and quality of vision (QoV questionnaire)
Time frame
Preoperatively, one, three and six monthsSponsors and contacts
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Source ClinicalTrials.gov