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Evaluation of Two Different Designs of Bausch & Lomb Contact Lenses

NCT01118338 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 376

Last updated 2020-10-06

Study results available
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Summary

The objective of this one month study is to evaluate the product performance of a redesigned PureVision Contact Lens compared to the PureVision Contact Lens when worn on a daily wear basis by wearers of contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

Redesigned Purevision Contact Lens

Lenses will be dispensed at screening visit, subjects will wear lenses on a daily wear basis for one month.

DEVICE

PureVision Contact Lens

Lenses will be dispensed at screening visit, subjects will wear lenses on a daily wear basis for one month.

Sponsors & Collaborators

  • Bausch & Lomb Incorporated

    lead INDUSTRY

Principal Investigators

  • Gerard Cairns, MCOptom, PhD · Bausch & Lomb Incorporated

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2010-06-30
Completion
2010-07-31

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 NCT01118338 on ClinicalTrials.gov