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Multi-Center 2-Week Clinical Evaluation of Three Silicone Hydrogel Contact Lenses

NCT01244516 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 540

Last updated 2018-06-19

Study results available
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Summary

The purpose of this study is to compare the clinical performance of three silicone hydrogel contact lenses over a 2 week period.

Conditions

  • Myopia

Interventions

DEVICE

galyfilcon A, BC 8.30

galyfilcon A, BC 8.30 soft contact lens

DEVICE

lotrafilcon B, BC 8.60

lotrafilcon B, BC 8.60 soft contact lens

DEVICE

comfilcon A, BC 8.60

comfilcon A, BC 8.60 soft contact lens

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2010-09-01
Primary Completion
2010-11-01
Completion
2010-11-01

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 NCT01244516 on ClinicalTrials.gov