Comparing Visual Outcomes in Matched Patients Receiving a Low Cylinder Power Toric IOL or a Non-toric IOL

Ifocus Oyeklinikk

Status: Completed

Conditions: Cataract and IOL Surgery

Treatments: Device: non-toric IOL implantation; Device: low cylinder toric IOL

Study type: Interventional

Funder types: NETWORK; Industry

Identifiers

NCT06717607

370677 (Other Identifier)

KGG-2021-01

Details and patient eligibility

About

The purpose of the study is to determine if visual function is improved with implantation of a low-cylinder toric intraocular lens, relative to a non-toric intraocular lens.

Full description

The Clareon(R) T2 IOL and the Clareon (R) non-toric IOL will be randomly implanted in subjects determined to be appropriate for the T2 IOL. Visual acuity, low contrast acuity and contrast sensitivity will be measured 3 months postoperatively.

Enrollment: 43 patients

Sex: All

Ages: 40+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• candidate for cataract surgery, suitable for implantation with a low cylinder toric IOL

Exclusion criteria

• pathology that would confound outcomes, previous ocular surgery

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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43 participants in 2 patient groups

Clareon T2 IOL implantation

Experimental group

Description:

low cylinder toric IOL

Treatment:

Device: low cylinder toric IOL

Clareon non-toric IOL implantation

Active Comparator group

Description:

Non-toric IOL

Treatment:

Device: non-toric IOL implantation