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Comparison of two aspheric Intraocular lenses used in cataract surgery- A Randomised Clinical Trial

Phase 3
Completed
Conditions
Health Condition 1: null- PATIENTS PLANNED FOR ROUTINE CATARACT SURGERYHealth Condition 2: H259- Unspecified age-related cataract
Registration Number
CTRI/2013/12/004198
Lead Sponsor
AIIMS
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
200
Inclusion Criteria

Age related senile cataract

No ocular problems or previous ocular surgery

No systemic contraindication

Exclusion Criteria

Any anterior segment pathology (chronic uveitis, iritis, iridocyclitis, rubeosis iridis, corneal dystrophy)

Complicated cataract

Bilateral congenital cataract

Posterior segment pathology

Systemic conditions (diabetes mellitus, systemic hypertension)

Posterior capsular rupture or zonular dialysis at the time of surgery

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Visual AcuityTimepoint: 1 month, 3 months, 6 months, 1 year
Secondary Outcome Measures
NameTimeMethod
Glare acuity, Contrast sensitivity, Posteroir vapsular opacification (PCO) rate, Ocular aberrationsTimepoint: 1 month, 3 months, 6 months, 1 year
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