CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 71 enrolled
Drug / intervention
ocufilcon D +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/NCT01464255
NCT01464255N/ACompleted

Clinical Performance of Ocufilcon D With a Wetting Agent to Ocufilcon B

CooperVision, Inc.·interventional·Posted Nov 3, 2011·Updated Aug 19, 2014

In Brief

A clinical study evaluating ocufilcon D and ocufilcon B for Myopia. Completed, enrolled 71 participants across 1 site.

Detailed Summary

This study is designed to evaluate ocufilcon D lens compared to ocufilcon B lens in a 1-week crossover, daily wear regimen.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedNov 3, 2011
Enrollment StartAug 1, 2011
Primary CompletionOct 1, 2011
Study CompletionNov 1, 2011
TodayJul 2, 2026
Enrollment to primary: 2 monthsPosted 14.7 years ago

Interventions

ocufilcon Ddevice

Participants wear a first pair of lenses for one week and then crossover and wear an alternate second pair of lenses for one week.

ocufilcon Bdevice

Participants wear a first pair of lenses for one week and then crossover and wear an alternate second pair of lenses for one week.