An interventional study of PRK and SBK in Myopia, sponsored by University of Utah. Completed at 1 site in United States. Open to participants aged 21 Years to 80 Years. Per ClinicalTrials.gov, last updated 2010-09-16.
Sponsored by University of Utah · Not applicable, Interventional, and Treatment
The objective of the study is to compare clinical outcomes from PRK and SBK using FDA-approved laser technology in the same patient
Patients undergoing bilateral laser refractive surgery on the same day will be randomly assigned to have one eye treated with PRK and the fellow eye treated with SBK.
984 studies on the registry are indexed under Myopia; 210 are open to participants now.
This study's enrollment of 60 is below the median of 80 across 783 interventional studies indexed under Myopia.
Browse Myopia studies →University of Utah is the lead sponsor of 969 studies on the registry; 178 are open to participants now.
Of its 107 completed or terminated interventional studies of FDA-regulated products, 62 (58%) have results posted.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
PRK
Procedure: PRK
SBK
Procedure: SBK
Laser refractive surgery
Laser refractive surgery
Visual acuity
Time frame: 6 months
Manifest refraction
Time frame: 6 months
Wavefront aberration value
Time frame: 6 months
This study is completed, as verified in Sep 2010. You cannot join it, but the record below documents what was studied.
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University of Utah