Comparison of LASIK and SBK

Not Applicable

Completed

• Conditions: Myopia
• Interventions: Procedure: SBK; Procedure: LASIK

• Registration Number: NCT00714363
• Lead Sponsor: University of Utah

Brief Summary

The objective of the study is to compare clinical outcomes from LASIK and SBK using FDA-approved laser technology on the same patient

Detailed Description

Patients undergoing bilateral refractive surgery on the same day will have one eye randomized to LASIK and the fellow eye assigned to SBK treatment.

Study Timeline

• Study Start: 2007-10
• Study First Submitted: 2008-07-08
• Study First Submitted QC: 2008-07-08
• Study First Posted: 2008-07-14
• Primary Completion: 2008-12
• Study Completion: 2010-01
• Status Verified: 2010-10
• Last Update Submitted: 2010-10-15
• Last Update Posted: 2010-10-19

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Patients deemed to be suitable candidates for bilateral LASIK surgery

Exclusion Criteria

• Patients who desire monovision correction rather than bilateral distance correction

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
2	SBK	SBK
1	LASIK	LASIK

Primary Outcome Measures

Name	Time	Method
Visual acuity	6 months

Secondary Outcome Measures

Name	Time	Method
Manifest refraction	6 months
Wavefront aberration value	6 months

Trial Locations

Locations (1)

University of Utah, John Moran Eye Center; 🇺🇸 Salt Lake City, Utah, United States