An interventional study of LASIK 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 2010-10-19.
Sponsored by University of Utah · Not applicable, Interventional, and Treatment
The objective of the study is to compare clinical outcomes from LASIK and SBK using FDA-approved laser technology on the same patient
Patients undergoing bilateral refractive surgery on the same day will have one eye randomized to LASIK and the fellow eye assigned to SBK treatment.
984 studies on the registry are indexed under Myopia; 210 are open to participants now.
This study's enrollment of 40 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:
LASIK
Procedure: LASIK
SBK
Procedure: SBK
Refractive surgery
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 Oct 2010. You cannot join it, but the record below documents what was studied.
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University of Utah