CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 29 enrolled
Drug / intervention
lotrafilcon 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/NCT01482312
NCT01482312N/ACompleted
CompareCT.gov

Effect of Contact Lenses on Tear Osmolarity in a Controlled Low Humidity Chamber

CIBA VISION·interventional·Posted Nov 30, 2011·Updated Jul 27, 2012

In Brief

A clinical study evaluating lotrafilcon A contact lenses, comfilcon A contact lenses, and 1 other intervention for Myopia and Dry Eye. Completed, enrolled 29 participants across 1 site.

Detailed Summary

The purpose of this study is to evaluate two different types of contact lenses and their effect on dry eyes when compared to wearing glasses in a controlled, low humidity chamber.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia, Dry Eye
CountriesCanada
Collaborators--

Timeline

N/ACompletedFinished
2011201220132014201520162017201820192020202120222023202420252026
First PostedNov 30, 2011
Enrollment StartDec 1, 2010
Primary CompletionFeb 1, 2011
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 14.6 years ago

Interventions

lotrafilcon A contact lensesdevice

Commercially marketed, silicone hydrogel, single-vision, soft contact lenses FDA-approved for daily and extended (overnight) wear for up to 30 nights of continuous wear.

comfilcon A contact lensesdevice

Commercially marketed, silicone hydrogel, single-vision, soft contact lenses FDA-approved for daily and extended (overnight) wear for up to 30 nights of continuous wear.

Glassesother

Glasses per habitual prescription