CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 144 enrolled
Drug / intervention
Dual Focus Soft Contact Lens +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/NCT01729208
NCT01729208N/ACompleted

A Multicentre Dispensing Clinical Evaluation of MiSight® Lenses

CooperVision, Inc.·interventional·Posted Nov 20, 2012·Updated Feb 24, 2020

In Brief

A clinical study evaluating Dual Focus Soft Contact Lens and Single Vision Soft Contact Lens for Myopia. Completed, enrolled 144 participants across 4 sites in 4 countries.

Detailed Summary

The purpose of this study is to determine whether a new type of soft contact lens with a unique optical design (dual focus) is effective at slowing the progression of myopia (near-sightedness) in children.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesCanada, Portugal, Singapore, United Kingdom

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedNov 20, 2012
Enrollment StartNov 1, 2012
Primary CompletionMay 1, 2017
Study CompletionMay 1, 2019
TodayJul 2, 2026
Enrollment to primary: 4.5 yearsPosted 13.6 years ago

Interventions

Dual Focus Soft Contact Lensdevice

Single Vision Soft Contact Lensdevice