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A Comparison of Two Contact Lenses

NCT00700752 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2015-05-21

Study results available
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Summary

This study seeks to evaluate the clinical and subjective performance of two established soft contact lenses.

Conditions

  • Refractive Error
  • Myopia

Interventions

DEVICE

senofilcon A

silicone hydrogel contact lens

DEVICE

balafilcon A

silicone hydrogel contact lens

Sponsors & Collaborators

  • 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
2008-05-31
Primary Completion
2008-07-31
Completion
2008-07-31

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 NCT00700752 on ClinicalTrials.gov