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A Comparison of Two Daily Disposable Contact Lenses

NCT00600080 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2015-05-21

Study results available
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Summary

This study seeks to evaluate the clinical performance of a recently improved daily disposable contact lens to an established daily disposable contact lens that contains a wetting agent.

Conditions

  • Myopia

Interventions

DEVICE

etafilcon A

contact lens worn daily for one week (first or second week depending on arm)

DEVICE

nelfilcon A

Contact lens worn daily for one week (first or second week depending on arm)

Sponsors & Collaborators

  • University of Manchester

    collaborator OTHER

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2008-03-31
Completion
2008-03-31

Countries

  • United Kingdom

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 NCT00600080 on ClinicalTrials.gov