Investigation of Corneal Aberrations and Visual Outcomes in Patients Implanted With an AcrySof Toric Intraocular Lens (IOL)

Alcon

Status: Withdrawn

Conditions: Astigmatism; Cataracts

Treatments: Device: Toric

Study type: Interventional

Funder types: Industry

Identifiers

NCT00878839

M09-016

Details and patient eligibility

About

A prospective evaluation of postoperative corneal aberrations and visual parameters (e.g. visual acuity) in patients implanted with an AcrySof Toric IOL.

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Operable cataracts;
• Good ocular health;
• Qualifies for AcrySof Toric IOL via AcrySof Toric Calculator (1.03-2.06 D cylinder at corneal plane)

Exclusion criteria

• >2.06 D astigmatism at corneal plane;
• irregular astigmatism;
• prior or ongoing corneal disease or scarring;
• history of ocular disease

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: None (Open label)

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0 participants in 1 patient group

Toric

Other group

Description:

AcrySof Toric IOL to assess corneal aberration

Treatment:

Device: Toric