Visual Performance of Bilateral AcrySof ReSTOR Aspheric +4

Alcon

Status: Completed

Conditions: Cataract

Treatments: Device: AcrySof ReSTOR Aspheric +4

Study type: Observational

Funder types: Industry

Identifiers

NCT01215045

M07-004

Details and patient eligibility

About

Determine the clinical visual outcomes following bilateral implantation of the AcrySof ReSTOR Aspheric Intraocular Lens (IOL) and to demonstrate what percentage of the subjects obtain spectacle freedom.

Enrollment: 17 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Diagnosed with cataracts

Exclusion criteria

• Preexisting conditions confounding results; > 1 Diopter preoperative astigmatism

Trial design

17 participants in 1 patient group

ReSTOR +4

Description:

AcrySof ReSTOR Aspheric +4

Treatment:

Device: AcrySof ReSTOR Aspheric +4