At a glance
ClinicalIndex Comparison RecordN/ACompleted· 22 enrolled
Drug / intervention
narafilcon B +3 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.
Daytime Corneal Swelling During Wear of Narafilcon B Lenses
In Brief
A clinical study evaluating narafilcon B, Polymacon, and 2 other interventions for Myopia. Completed, enrolled 22 participants across 1 site.
Detailed Summary
The purpose of this research is to measure daytime open-eye response to wearing of narafilcon B lenses.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesAustralia
Collaborators--
Timeline
N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
Enrollment StartJan 2010
Primary CompletionFeb 2010
Study CompletionMar 2010
First PostedSep 2011
TodayJul 2026
First PostedSep 30, 2011
Enrollment StartJan 1, 2010
Primary CompletionFeb 1, 2010
Study CompletionMar 1, 2010
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 14.8 years ago
Interventions
narafilcon Bdevice
test product
Polymacondevice
marketed product
Lotrafilcon Adevice
marketed product
Spectaclesother
None - subject used own spectacles