At a glance
ClinicalIndex Comparison RecordN/ACompleted· 19 enrolled
Drug / intervention
Delefilcon A contact lens +2 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.
A Comparative Study of Two Daily Disposable Contact Lenses in Higher Myopia Subjects
In Brief
A clinical study evaluating Delefilcon A contact lens, Narafilcon A contact lens, and 1 other intervention for Refractive Error and Myopia. Completed, enrolled 19 participants.
Detailed Summary
The purpose of this study is to compare the change from baseline in central corneal curvature at one week, between 2 silicone hydrogel lenses, in higher myopic subjects.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRefractive Error, Myopia
Countries--
Collaborators--
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedFeb 2014
Enrollment StartMar 2014
Primary CompletionMay 2014
TodayJul 2026
First PostedFeb 20, 2014
Enrollment StartMar 1, 2014
Primary CompletionMay 1, 2014
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 12.4 years ago
Interventions
Delefilcon A contact lensdevice
Commercially available silicone hydrogel contact lens
Narafilcon A contact lensdevice
Commercially available silicone hydrogel contact lens
Spectaclesdevice
Incremental prescription worn over contact lenses if needed to provide acceptable vision