MedTrace Logo

Evaluation of Daytime Corneal Swelling During Wear of Galyfilcon A Lenses

NCT01482819 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2018-06-19

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to evaluate corneal swelling, limbal redness, and endothelial bleb response to wearing galyfilcon A lenses in asian eyes.

Conditions

  • Myopia

Interventions

DEVICE

galyfilcon A

contact lenses worn bilaterally for 8-12 hours

DEVICE

galyfilcon A plus

contact lenses worn bilaterally for 8-12 hours

DEVICE

lotrafilcon A

contact lenses worn bilaterally for 8-12 hours

DEVICE

polymacon

contact lenses worn bilaterally for 8-12 hours

OTHER

spectacles

habitual spectacles owned by subject, non-specific manufacturer

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-10-01
Primary Completion
2011-12-01
Completion
2011-12-01

Countries

  • Australia

Study Locations

More Related Trials

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 NCT01482819 on ClinicalTrials.gov