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Clinical Performance of a New Daily Disposable Contact Lens Worn in an Established Contact Lens Wearing Population

NCT00708643 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2015-05-21

Study results available
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Summary

This study seeks to evaluate the clinical and subjective performance of a new daily disposable soft contact lens.

Conditions

  • Refractive Error
  • Myopia

Interventions

DEVICE

Habitual Silicone Hydrogel Contact Lens

contact lens

DEVICE

narafilcon A

contact lens

Sponsors & Collaborators

  • University of Manchester

    collaborator OTHER

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-06-30
Primary Completion
2008-09-30
Completion
2008-09-30

Countries

  • Canada

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 NCT00708643 on ClinicalTrials.gov