Comparison of Corneal Aberrations and Visual Outcomes in AcrySof IQ Toric Patients Versus Limbal Relaxing Incision (LRI) Patients

Alcon

Status and phase: Withdrawn; Phase 4

Conditions: Cataracts

Treatments: Device: Toric; Procedure: Limbal Relaxing Incision

Study type: Interventional

Funder types: Industry

Identifiers

NCT00929747

M08-008

Details and patient eligibility

About

A prospective evaluation of postoperative corneal aberrations and visual parameters in patients assigned to either an AcrySof IQ Toric intraocular lens (IOL) group or a group implanted with a SN60WF IOL and having concomitant limbal relaxing incision.

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. operable cataracts
2. good ocular health
3. 0.5 D to 2.0 D of corneal astigmatism

Exclusion criteria

1. > 2.0 D astigmatism
2. irregular astigmatism
3. prior or ongoing corneal disease or scarring
4. history of ocular disease

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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0 participants in 2 patient groups

Toric IOL

Active Comparator group

Description:

AcrySof IQ Toric IOL

Treatment:

Device: Toric

Limbal Relaxing Incision

Active Comparator group

Description:

AcrySof IQ with Limbal Relaxing Incision

Treatment:

Procedure: Limbal Relaxing Incision