At a glance
ClinicalIndex Comparison RecordN/ACompleted· 21 enrolled
Drug / intervention
galyfilcon A +4 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Evaluation of Daytime Corneal Swelling During Wear of Galyfilcon A Lenses
In Brief
A clinical study evaluating galyfilcon A, galyfilcon A plus, and 3 other interventions for Myopia. Completed, enrolled 21 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesAustralia
Collaborators--
Timeline
N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
Enrollment StartOct 2011
First PostedDec 2011
Primary CompletionDec 2011
TodayJul 2026
First PostedDec 1, 2011
Enrollment StartOct 1, 2011
Primary CompletionDec 1, 2011
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 14.6 years ago
Interventions
galyfilcon Adevice
contact lenses worn bilaterally for 8-12 hours
galyfilcon A plusdevice
contact lenses worn bilaterally for 8-12 hours
lotrafilcon Adevice
contact lenses worn bilaterally for 8-12 hours
polymacondevice
contact lenses worn bilaterally for 8-12 hours
spectaclesother
habitual spectacles owned by subject, non-specific manufacturer