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Performance Evaluation of Contact Lenses Among a Population of Adapted Contact Lens Wearers

NCT00985231 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 272

Last updated 2015-03-24

Study results available
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Summary

This study is being conducted to evaluate Bausch \& Lomb PureVision Multi-Focal contact lenses compared to the Bausch \& Lomb SofLens59 contact lens when worn by adapted soft contact lens wearers on a daily wear basis.

Conditions

  • Vision Disorders

Interventions

DEVICE

PureVision Multi-Focal contact lenses

Contact lenses to be worn on a daily wear basis for 2 weeks.

DEVICE

SofLens59 contact lens

Contact lenses to be worn on a daily wear basis for 2 weeks.

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Beverly J Barna · Bausch & Lomb Incorporated

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-30
Primary Completion
2009-11-30
Completion
2009-12-31

Countries

  • United States

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 NCT00985231 on ClinicalTrials.gov