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Visual Function After Implantation of AcrySof® Toric Lens

NCT01074606 · Status: TERMINATED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2012-09-19

No results posted yet for this study

Summary

The objective of this study is to evaluate the postoperative visual function of Taiwanese patients following bilateral or unilateral AcrySof Toric Intraocular Lens (IOL) implantation.

Conditions

  • Cataract

Interventions

DEVICE

AcrySof Toric Intraocular Lens

Implantation of the AcrySof Toric Intraocular Lens (IOL)

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2011-03-31

Countries

  • Taiwan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01074606 on ClinicalTrials.gov