NCT01482819

Evaluation of Daytime Corneal Swelling During Wear of Galyfilcon A Lenses

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 21 (actual)
• Sponsor: Johnson & Johnson Vision Care, Inc. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

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

Type	Name	Description
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

Timeline

• Start date: 2011-10-01
• Primary completion: 2011-12-01
• Completion: 2011-12-01
• First posted: 2011-12-01
• Last updated: 2018-06-19
• Results posted: 2015-04-30

Locations

1 site across 1 country: Australia