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Comparision of visual outcomes in patients following topography guided femtosecond laser-in-situ keratomileusis and small incision lenticule extractio

Not Applicable
Conditions
Health Condition 1: H578- Other specified disorders of eye and adnexa
Registration Number
CTRI/2020/12/029990
Lead Sponsor
V Prasad Eye Institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Myopia from -2.00 to -10 D and myopic astigmatism up to 1.5 D

2.Age more than 21 years

3.Corneal thickness at the thinnest point >500 microns

4.Stable refractive error (Change <0.50D) over the last 6 months

5.Discontinuation of contact lens for more than 2 weeks for soft contact lens and 3 weeks for rigid contact lens

6.No previous ocular surgery

7.Preoperative CDVA of atleast 20/25

Exclusion Criteria

1.Any surgery related complications affecting the outcome

2.Amblyopia

3.History of corneal dystrophy, herpetic eye disease, topographic evidence of keratoconus, epithelial warpage from contact lens use, corneal scarring, glaucoma, severe dry eye and collagen vascular disease.

4.Any other ocular comorbities that may affect the outcome

5.Participation in any other clinical trial at the time of conduct of the study

6.Refusal to adhere to visit dates and study protocols

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual AcuityTimepoint: day 1, 1st week, 1st month, and 3rd month.
Secondary Outcome Measures
NameTimeMethod
Severity of dry eye <br/ ><br>Light Sensitivity <br/ ><br>Vision related quality of lifeTimepoint: 1 week, 1 month and 3 months
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