Comparing two corneal topography systems for eligibility and suitability for premium intra-ocular lenses to be implanted during cataract surgery.
Not Applicable
- Conditions
- Health Condition 1: H251- Age-related nuclear cataract
- Registration Number
- CTRI/2021/11/038053
- Lead Sponsor
- CARL ZEISS MEDITEC
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
200 eyes of eligible patients undergoing unilateral or bilateral phacoemulsification with toric monofocal, multifocal or toric multifocal implants will be included in the study.
Exclusion Criteria
Patients undergoing cataract surgery with non-toric monofocal implants and general exclusion criteria for premium IOLs such as known or diagnosed cases of keratoconus, PPMD, post refractive surgery, retinal or macular pathologies, glaucoma, subluxated or traumatic cataracts etc.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Agreement between IOL Master 700 CT and Pentacam HR in detection of irregular cornea for evaluating the suitability for a premium IOL surgery.Timepoint: Baseline
- Secondary Outcome Measures
Name Time Method Reliability of IOL Master CT in identifying irregular corneasTimepoint: Baseline