CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 9 enrolled
Drug / intervention
delefilcon A contact lens +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.

Search/NCT01473160
NCT01473160N/ACompleted
CompareCT.gov

DAILIES TOTAL1 Pre-Lens Tear Film Performance - Pilot Trial

CIBA VISION·interventional·Posted Nov 17, 2011·Updated Apr 17, 2013

In Brief

A clinical study evaluating delefilcon A contact lens and narafilcon A contact lens for Myopia. Completed, enrolled 9 participants across 1 site.

Detailed Summary

The purpose of this study was to evaluate the pre-lens tear film stability of a new CE-marked daily disposable contact lens as compared to a commercially available daily disposable contact lens.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited Kingdom
CollaboratorsAston University

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedNov 17, 2011
Enrollment StartNov 1, 2011
Primary CompletionDec 1, 2011
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 14.6 years ago

Interventions

delefilcon A contact lensdevice

CE-marked, silicone hydrogel, single vision, soft contact lens for daily disposable wear

narafilcon A contact lensdevice

Commercially marketed, silicone hydrogel, single vision, soft contact lens for daily disposable wear.