CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 25 enrolled
Drug / intervention
lotrafilcon B +3 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/NCT01010555
NCT01010555N/ACompleted
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In-vivo Wettability Grading and Assessment Study

CIBA VISION·interventional·Posted Nov 10, 2009·Updated Jul 10, 2012

In Brief

A clinical study evaluating lotrafilcon B, balafilcon A, and 2 other interventions for Myopia. Completed, enrolled 25 participants across 1 site.

Detailed Summary

The purpose of this study is to investigate the front surface wettability of soft contact lenses while on eye.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesCanada
CollaboratorsUniversity of Waterloo

Timeline

N/ACompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedNov 10, 2009
Enrollment StartOct 1, 2009
Primary CompletionApr 1, 2010
TodayJul 2, 2026
Enrollment to primary: 6 monthsPosted 16.6 years ago

Interventions

lotrafilcon Bdevice

Commercially marketed, silicone hydrogel, spherical contact lens

balafilcon Adevice

Commercially marketed, silicone hydrogel, spherical contact lens

senofilcon Adevice

Commercially marketed, silicone hydrogel, spherical contact lens

enfilcon Adevice

Commercially marketed, silicone hydrogel, spherical contact lens