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A Comparison of Two Daily Disposable Contact Lenses

NCT00634101 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 129

Last updated 2021-01-06

Study results available
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Summary

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

Conditions

  • Refractive Error
  • Myopia

Interventions

DEVICE

nelfilcon A

contact lens

DEVICE

narafilcon A

contact lens

Sponsors & Collaborators

  • Visioncare Research Ltd.

    collaborator OTHER

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-01
Primary Completion
2008-03-01
Completion
2008-03-01
FDA Device
Yes

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 NCT00634101 on ClinicalTrials.gov