At a glance
ClinicalIndex Comparison RecordN/ACompleted· 62 enrolled
Drug / intervention
Delefilcon A contact lenses +1 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.
Impact of a Novel Silicone Hydrogel in Reducing Contact Lens-Related Dryness Symptoms in Existing Contact Lens Wearers
In Brief
A clinical study evaluating Delefilcon A contact lenses and Etafilcon A contact lenses for Myopia. Completed, enrolled 62 participants.
Detailed Summary
The purpose of this study was to evaluate the performance of a novel silicone hydrogel contact lens, DAILIES TOTAL1® (DT1) compared to the standard hydrogel material in 1-DAY ACUVUE® MOIST® (1DAVM) contact lens in contact lens wearers identified as having contact lens-related dryness symptoms.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
Countries--
Collaborators--
Timeline
N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
Enrollment StartJul 2012
First PostedJul 2012
Primary CompletionNov 2012
TodayJul 2026
First PostedJul 10, 2012
Enrollment StartJul 1, 2012
Primary CompletionNov 1, 2012
TodayJul 2, 2026
Enrollment to primary: 4 monthsPosted 14.0 years ago
Interventions
Delefilcon A contact lensesdevice
Silicone hydrogel contact lenses for daily wear, daily disposable use
Etafilcon A contact lensesdevice
Hydrogel contact lenses for daily wear, daily disposable use