AcrySof Toric Clinical Results

Completed

• Conditions: Cataracts; Astigmatism
• Interventions: Device: T3; Device: T4; Device: T5

• Registration Number: NCT01214863
• Lead Sponsor: Alcon Research

Brief Summary

This study is an evaluation of visual outcomes of subjects implanted with the AcrySof Toric Intraocular Lenses (IOLs) Models SN60T3, SN60T4, and SN60T5.

Detailed Description

Not available

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

Study Timeline

• Study Start: 2007-08
• Primary Completion: 2008-04
• Study First Submitted: 2008-08-07
• Status Verified: 2010-10
• Study First Submitted QC: 2010-10-04
• Study First Posted: 2010-10-05
• Last Update Submitted: 2012-09-27
• Last Update Posted: 2012-10-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 144

Inclusion Criteria

• Diagnosed with cataracts; has astigmatism falling in range of AcrySof Toric lens as assessed by the AcrySof Toric calculator

Read More

Exclusion Criteria

• Ocular comorbidities affecting visual outcome data,
• Prior refractive surgery,
• Irregular astigmatism

Read More

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
T3	T3	Model SN60T3 assigned by AcrySof Toric calculator
T4	T4	Model SN60T4 assigned by AcrySof Toric calculator
T5	T5	Model SN60T5 assigned by AcrySof Toric calculator

Primary Outcome Measures

Name	Time	Method
Visual Acuity	1 day to 6 months

Secondary Outcome Measures

Name	Time	Method
Postoperative refractive cylinder	1day to 6 months

Trial Locations

Locations (1)

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