Comparing standard myopic LASIK to contralateral eye LASIK customised with a novel software already EU approved

Not Applicable

• Conditions: Treatment of myopic refractive error with LASIK; Eye Diseases

• Registration Number: ISRCTN73528436
• Lead Sponsor: aserVision

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2023-09-14
• Last Update Posted: 26 September 2023
• Study Completion: 2023-12-31

Recruitment & Eligibility

• Status: Ongoing
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

Adults undergoing refractive error laser correction with no other corneal/ocular pathology (ie. Keratoconus, Pterygium) other than refractive error

Exclusion Criteria

Corneal/Ocular pathology other than refractive error

Study & Design

• Study Type: Observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<br> 1. Pre- and Post- operation mean refractive error is measured with an autorefractor<br> 2. Topographic astigmatism is measured using keratometry at Pre- and Post- operation<br>

Secondary Outcome Measures

Name	Time	Method
Visual Acuity is measured using the Snellen chart at Pre- and Post- operation