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A Study to Evaluate the Performance of Two Designs of Soft Toric Lenses

NCT01309867 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 302

Last updated 2020-10-08

Study results available
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Summary

The objective of the study is to evaluate the product performance of the Bausch + Lomb toric investigational contact lenses compared to the currently marketed PureVision toric contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

Investigational Toric Lens

Bausch \& Lomb investigational toric contact lens worn on a daily wear basis for 2 weeks.

DEVICE

PureVision Toric Lens

Currently marked Bausch \& Lomb PureVision Toric Lens worn on a daily wear basis for 2 weeks.

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Beverly Barna · Bausch & Lomb Incorporated

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-12-31
Primary Completion
2011-02-28
Completion
2011-04-30

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 NCT01309867 on ClinicalTrials.gov