Surgeon Experience ReSTOR A +4 Intraocular Lens (IOL)

Alcon

Status: Completed

Conditions: Cataract

Treatments: Device: ReSTOR

Study type: Observational

Funder types: Industry

Identifiers

NCT00733512

M07-019

Details and patient eligibility

About

To collect visual outcome data post AcrySof ReSTOR Aspheric +4 implantation from surgeons throughout the United States.

Enrollment: 146 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• operable cataracts; candidate for presbyopic correcting intraocular lens (IOL)

Exclusion criteria

• ocular comorbidities confounding study outcomes

Trial design

146 participants in 1 patient group

ReSTOR

Description:

AcrySof ReSTOR Aspheric +4 Intraocular Lens (IOL)

Treatment:

Device: ReSTOR