This clinical trial is to study the digital method for eye lens to be placed during cataract surgery by comparing with the manual method
Phase 4
- Conditions
- Health Condition 1: H252- Age-related cataract, morgagnian typeHealth Condition 2: H259- Unspecified age-related cataract
- Registration Number
- CTRI/2024/04/065250
- Lead Sponsor
- Center for Application Research in India (CARIn) Carl Zeiss India
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Subjects with regular corneal astigmatism greater than 0.75D willing to undergo cataract extraction. Patient willing to undergo cataract surgery with implantation of an Toric intraocular lenses. Patient giving full and free consent for involvement in the study. Patient willing to come for follow up study visits and measurements.
Exclusion Criteria
Any ocular pathology or degeneration that could have impact on vision and/or a contradiction to Toric IOL implantation.
Any surgical complication felt to in any way impact upon the quality of visual outcome.
Any other comorbid conditions or risk factors that may affect the surgical procedure.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method One-month postoperative refractionTimepoint: 1 week and 1 month
- Secondary Outcome Measures
Name Time Method ncorrected & best corrected visual acuity by log MAR visual acuity 1 month. IOL axis alignment, immediate postop, 1 day postop & 1 month postop.Timepoint: 1 week & 1 month.