Visual Performance of Bilateral AcrySof ReSTOR Aspheric +4

Alcon Research1 site in 1 country17 target enrollmentStarted: June 2007Last updated: October 5, 2010

Conditions

Trial Snapshot

Phase: Not Applicable
Status: Completed
Sponsor: Alcon Research
Enrollment: 17
Locations: 1
Primary Endpoint: Visual Acuity

Study Overview Study Design Eligibility Criteria Outcomes Investigators Sites Records & Identifiers Similar Trials

Study Overview

Brief Summary

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.

Study Design

Study Type: Observational
Observational Model: Case Only
Time Perspective: Prospective

Eligibility Criteria

Ages: 18 Years to 70 Years (Adult, Older Adult)
Sex: All
Accepts Healthy Volunteers: Yes

Inclusion Criteria

•Diagnosed with cataracts

Exclusion Criteria

•Preexisting conditions confounding results; > 1 Diopter preoperative astigmatism

Outcomes

Primary Outcomes

Visual Acuity

Time Frame: 6 months

Secondary Outcomes

Contrast sensitivity, patient survey(6 months)

Investigators

Sponsor

Alcon Research

Sponsor Class

Industry

Study Sites (1)

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