CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 70 enrolled
Drug / intervention
filcon II 3 +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/NCT02094677
NCT02094677N/ACompleted

Daily Disposable Comparison Study

CooperVision, Inc.·interventional·Posted Mar 24, 2014·Updated Jul 28, 2020

In Brief

A clinical study evaluating filcon II 3, etafilcon A, and 1 other intervention for Myopia. Completed, enrolled 70 participants across 1 site.

Detailed Summary

The objective of the study is to compare the overall subjective preference between two Daily Disposable hydrogel lenses when refitted into a third hydrogel lens.

Study Details

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

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedMar 24, 2014
Enrollment StartMar 1, 2014
Primary CompletionApr 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1 monthPosted 12.3 years ago

Interventions

filcon II 3device

Participants were randomized to wear filcon II 3 test lens.

etafilcon Adevice

Participants were randomized to wear etafilcon A control lens.

nelfilcon Adevice

Participants were randomized to wear nelfilcon A control lens.