Rotational Stability of the AcrySof® Toric

Alcon

Status: Completed

Conditions: Cataract

Treatments: Device: AcrySof® Toric intraocular lens

Study type: Interventional

Funder types: Industry

Identifiers

NCT00762216

RM-08-001

Details and patient eligibility

About

To assess the rotational stability and the residual refractive cylinder and patient reported outcomes of the AcrySof Toric intraocular lens after unilateral or bilateral implantation.

Enrollment: 71 patients

Sex: All

Ages: 40 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Monolateral or bilateral cataracts
• anticipated intraocular lens (IOL) power of +10 Diopters (D) ~ +25D
• 0.75 ~ 2.0 D of astigmatism measured preoperatively by Keratometry readings
• able to sign the informed consent, to comply with scheduled visits and other study procedures

Exclusion criteria

• Preoperative ocular pathology
• previous intraocular or corneal surgery
• an increased risk for complications which could require vitreoretinal surgery
• corneal irregularities
• corneal opacities
• current contact lens usage
• uncontrolled diabetes

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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71 participants in 1 patient group

Toric

Other group

Description:

Implantation with the AcrySof® Toric intraocular lens

Treatment:

Device: AcrySof® Toric intraocular lens