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to study the effect of preservative free drug- eye drop to reduce pain in patients undergoing laser eye surgery to correct refractive errors

Not Applicable
Conditions
Health Condition 1: null- myopia , astigmatism refractive error
Registration Number
CTRI/2016/01/006536
Lead Sponsor
ethradhama super speciality eye hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
50
Inclusion Criteria

Spherical equivalent from -1 to -6 D.

Stable refraction at least for the previous 1 year.

Soft Contact lenses will have to be discontinued for minimum 1 week and rigid gas permeable contact lens discontinued for minimum 3 weeks before the baseline measurement

Exclusion Criteria

1.Age less than 21 years and more than 40 years.

2.Evidence of lid diseases like meibomian gland dysfunction.

3.Anterior segment pathologies of the cornea like corneal dystrophy, corneal scars, keratitis, topographic evidence of keratoconus. Residual, recurrent or active ocular disease such as uveitis, severe dry eyes, severe allergic eye disease, glaucoma, visually significant cataract.

4.Retinal pathologies like diabetic retinopathy and retinal dystrophies.

5.Progressive or unstable myopia and/or irregular astigmatism.

6.Previous intraocular or corneal surgery.

7.Ocular medications being used like antiglaucoma medications.

8.Systemically immunocompromised.

9.Pregnant or nursing women

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
pain scoresTimepoint: day1,3,5
Secondary Outcome Measures
NameTimeMethod
eye discomfortTimepoint: day1,3,5
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