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Evaluation of Deposits on Contact Lenses Worn Daily Wear

NCT00725153 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 55

Last updated 2012-08-23

Study results available
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Summary

The purpose of this study was to measure front surface deposits on contact lenses when worn for ten hours.

Conditions

  • Refractive Error

Interventions

DEVICE

Balafilcon A contact lenses (PureVision)

Commercially marketed, soft contact lenses worn bilaterally for 10 hours

DEVICE

Etafilcon A contact lenses (Acuvue2)

Commercially marketed, soft contact lenses worn bilaterally for 10 hours

Sponsors & Collaborators

  • Alcon Research

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2008-09-30
Completion
2008-09-30

Countries

  • United States

Study Locations

More Related Trials

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 NCT00725153 on ClinicalTrials.gov