Comparison of Conventional and Custom Photorefractive Keratectomy (PRK)

Completed · Not applicable

Conditions studied: Myopia

In brief

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.

Key facts

Study ID
NCT00713856
Run by
University of Utah
People needed
44
Starts
2007-11-01
Expected to finish
2010-05-01
Last updated by the study team
2010-10-19

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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