About this trial
To evaluate the clinical outcomes and patient satisfaction of two commercially available trifocal toric intraocular lenses Primary Objective: To compare the distance-corrected intermediate visual acuity between the two trifocal toric intraocular lenses. Secondary Objectives: To assess and compare the safety of two trifocal toric intraocular lenses.
Eligibility criteria
Qualifiers
Age of patient >21 Years
Patient diagnosed with cataract.
Patient must have preoperative regular corneal astigmatism between 0.75 to 4.5 D as per corneal topography or keratometry
Calculated IOL power is within the range of investigational IOLs.
Disqualifiers
Previous intraocular or corneal surgery.
Traumatic cataract
Pregnancy (as stated by patient) or lactation.
Concurrent participation in another drug or device investigation.
Trial design
Treatments tested in this trial
- Optiflex TRIO Intraocular Lens
- AcrySof® IQ PanOptix®