University of Utah, John Moran Eye Center
Salt Lake City, Utah, 84106, United States
NCT Number: NCT00714922
The objective of the study is to compare clinical outcomes from PRK and SBK using FDA-approved laser technology in the same patient
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Notify Me21 year–80 year
All sexes
Interventional
Not applicable
Salt Lake City, Utah, 84106, United States
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Laser refractive surgery
Laser refractive surgery
Time frame: 6 months
Time frame: 6 months
Time frame: 6 months
University of Utah
Other
Comparison of Photorefractive Keratectomy (PRK) and Sub-Bowman's Keratomileusis (SBK): Assessment of Visual Function and Patient Satisfaction
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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