Visual Performance of Bilateral AcrySof ReSTOR Aspheric +4

Completed

• Conditions: Cataract
• Interventions: Device: AcrySof ReSTOR Aspheric +4

• Registration Number: NCT01215045
• Lead Sponsor: Alcon Research

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.

Detailed Description

Not available

Basic Information
|
Recruitment & Eligibility
|
Study & Design
|
Trial Locations

Study Timeline

• Study Start: 2007-06
• Primary Completion: 2008-05
• Study Completion: 2008-05
• Study First Submitted: 2008-08-12
• Status Verified: 2010-10
• Study First Submitted QC: 2010-10-04
• Last Update Submitted: 2010-10-04
• Study First Posted: 2010-10-05
• Last Update Posted: 2010-10-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 17

Inclusion Criteria

• Diagnosed with cataracts

Read More

Exclusion Criteria

• Preexisting conditions confounding results; > 1 Diopter preoperative astigmatism

Read More

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
ReSTOR +4	AcrySof ReSTOR Aspheric +4	AcrySof ReSTOR Aspheric +4

Primary Outcome Measures

Name	Time	Method
Visual Acuity	6 months

Secondary Outcome Measures

Name	Time	Method
Contrast sensitivity, patient survey	6 months

Trial Locations

Locations (1)

Contact Alcon Call Center for Trial Locations; 🇺🇸 Fort Worth, Texas, United States