CLINICAL OUTCOMES OF DIFFERENT MULTIFOCAL TORIC IOLs IN ONE YEAR PROSPECTIVE CLINICAL STUDY
- Conditions
- Health Condition 1: H259- Unspecified age-related cataract
- Registration Number
- CTRI/2019/10/021676
- Lead Sponsor
- Dr Sri Ganesh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1. Patients who has been implanted bilaterally with the Multifocal Toric IOL will be included in the Study.
2. Age 18 and older
3. Regular corneal topography and corneal astigmatism more than 0.75 D.
4. Best Corrected Visual Acuity to be 0.2 LogMAR or Lower
5. Clear intraocular media
6. Availability, willingness and sufficient cognitive awareness to comply with examination procedures
7. Patients who has given informed written consent.
1. Any active ocular disease (Diabetic retinopathy, macular degeneration, glaucoma with field defects and irregular corneal astigmatism)
2. Previous intraocular and corneal surgery
3. Pregnancy & Lactation
4. Traumatic Cataract
5. Subject who are expected to required retinal laser treatment
Concurrent participation in another drug or device Study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual acuity (UCDVA & BCDVA).Visual acuity (Near & Intermediate).Toric Marks Measurement (Rotational Stability) using Itrace.Refractive astigmatism.Spherical EquivalentTimepoint: Preoperative Visit.Intraoperative Visit.Postoperative 1 Day.Postoperative 7 Days.Postoperative 30 Days.Postoperative 90 Days.Postoperative 180 Days.Postoperative 365 Days
- Secondary Outcome Measures
Name Time Method Intraocular Pressure (IOP).Endothelial Cell Count.Pupil Size.Defocus CurveCorrected up to ± 4 D.Timepoint: Preoperative Visit.Intraoperative Visit.Postoperative 1 Day.Postoperative 7 Days.Postoperative 30 Days.Postoperative 90 Days.Postoperative 180 Days.Postoperative 365 Days