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Evaluation of the effect of LASIK on axial length

Not Applicable
Conditions
High myopia
Registration Number
JPRN-UMIN000023081
Lead Sponsor
Baptist Eye Institute
Brief Summary

A paired t-test was used to examine the amount of axial length elongation for two years, and the result was 0.08mm in the LASIK group and 0.06mm in the soft contact lens group, showing no difference between the two groups. At 2.5 years after surgery, uncorrected visual acuity in the LASIK group was 1.40, corrected visual acuity was 1.57, efficacy index was 1.01, safety index was 1.15, and subjective refraction was -0.16D.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
22
Inclusion Criteria

Not provided

Exclusion Criteria

(1)keratoconus (2)active ocular outer inflammation (3)cataract (4)inflammation with uveitis and scleritis (5)the whole body with a high possibility that I have an influence on a wound healing or immunodeficient disease such as serious case's diabetes and serious case's atopic disease (6)during pregnancy or nursing lady (7)keratoconus suspect (8)additionally the study person in charge judges participation in this research to be unsuitable

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Axial length
Secondary Outcome Measures
NameTimeMethod
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