CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 37 enrolled
Drug / intervention
Delefilcon A contact lenses +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.

Search/NCT02517567
NCT02517567N/ACompleted
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Pilot Study on the Effect of Daily Disposable Silicone Hydrogel Contact Lenses on Tear Film Lipids

Alcon Research·interventional·Posted Aug 7, 2015·Updated Jul 2, 2018

In Brief

A clinical study evaluating Delefilcon A contact lenses, Narafilcon A contact lenses, and 1 other intervention for Refractive Error. Completed, enrolled 37 participants.

Detailed Summary

The purpose of this study is to evaluate the tear film evaporation of symptomatic soft contact lens wearers in the absence of contact lens wear and after at least 8 hours of contact lens wear.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsRefractive Error
Countries--
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedAug 7, 2015
Enrollment StartSep 21, 2015
Primary CompletionApr 22, 2016
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 10.9 years ago

Interventions

Delefilcon A contact lensesdevice

Daily disposable, silicone hydrogel contact lenses used according to manufacturer's instructions

Narafilcon A contact lensesdevice

Daily disposable, silicone hydrogel contact lenses used according to manufacturer's instructions

Somofilcon A contact lensesdevice

Daily disposable, silicone hydrogel contact lenses used according to manufacturer's instructions