CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 119 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.

Search/NCT01371552
NCT01371552N/ACompleted

Performance Evaluation of a New Daily Disposable Silicone Hydrogel Lens (TUNGSTEN)

CIBA VISION·interventional·Posted Jun 13, 2011·Updated Oct 31, 2012

In Brief

A clinical study evaluating delefilcon A contact lens, filcon II 3 contact lenses, and 1 other intervention for Myopia. Completed, enrolled 119 participants across 1 site.

Detailed Summary

The purpose of this study was to compare a new daily disposable, silicone hydrogel contact lens to marketed daily disposable, silicone hydrogel contact lenses.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesCanada
Collaborators--

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedJun 13, 2011
Enrollment StartMay 1, 2011
Primary CompletionAug 1, 2011
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 15.1 years ago

Interventions

delefilcon A contact lensdevice

Investigational, silicone hydrogel, single vision contact lens worn on a daily disposable basis for 3 days in Part 1 and one week in Part 2.

filcon II 3 contact lensesdevice

Commercially marketed, silicone hydrogel, single vision contact lens worn on a daily disposable basis for 3 days in Part 1.

narafilcon A contact lensesdevice

Commercially marketed, silicone hydrogel, single vision contact lens worn on a daily disposable basis for 3 days in Part 1.