Status:
COMPLETED
Comparison of Conventional and Custom Photorefractive Keratectomy (PRK)
Lead Sponsor:
University of Utah
Conditions:
Myopia
Eligibility:
All Genders
18-80 years
Phase:
NA
Brief Summary
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.
Detailed Description
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.
Eligibility Criteria
Inclusion
- Patients deemed to be suitable candidates for bilateral PRK
Exclusion
- Patients desiring monovision correction rather than bilateral distance correction
Key Trial Info
Start Date :
November 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2010
Estimated Enrollment :
44 Patients enrolled
Trial Details
Trial ID
NCT00713856
Start Date
November 1 2007
End Date
May 1 2010
Last Update
October 19 2010
Active Locations (1)
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1
University of Utah, John Moran Eye Center
Salt Lake City, Utah, United States, 84132