Expired Study
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Salt Lake City, Utah 84132


Purpose:

The study objective is to compare the clinical outcomes using wavefront guided PRK with iris registration and conventional laser PRK using FDA-approved laser technology on the same patient.


Study summary:

Patients undergoing bilateral PRK on the same day will have one eye randomly assigned to custom wavefront guided PRK and the fellow eye treated with conventional PRK.


Criteria:

Inclusion Criteria: - Patients deemed to be suitable candidates for bilateral PRK Exclusion Criteria: - Patients desiring monovision correction rather than bilateral distance correction


NCT ID:

NCT00713856


Primary Contact:

Principal Investigator
Mark Mifflin, MD
University of Utah


Backup Contact:

N/A


Location Contact:

Salt Lake City, Utah 84132
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

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