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…
- Patients deemed to be suitable candidates for bilateral PRK
You may not qualify if…
- Patients desiring monovision correction rather than bilateral distance correction
Where it is running
- University of Utah, John Moran Eye Center — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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