CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 83 enrolled
Drug / intervention
Single Vision Soft Contact Lensdevice
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/NCT05779072
NCT05779072N/ACompleted
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MiSight Lens Wear Cessation Study

CooperVision, Inc.·interventional·Posted Mar 22, 2023·Updated Nov 1, 2023

In Brief

A clinical study evaluating Single Vision Soft Contact Lens for Myopia. Completed, enrolled 83 participants across 4 sites in 4 countries.

Detailed Summary

The purpose of this study is to investigate the effect of ceasing treatment with dual focus soft contact lenses.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMyopia
CountriesCanada, Portugal, Singapore, United Kingdom
CollaboratorsVisioncare Research Ltd.

Timeline

N/ACompletedFinished
20192020202120222023202420252026
First PostedMar 22, 2023
Enrollment StartMar 1, 2019
Primary CompletionMar 1, 2021
TodayJul 2, 2026
Enrollment to primary: 2 yearsPosted 3.3 years ago

Interventions

Single Vision Soft Contact Lensdevice

Subjects refit to Single Vision Soft Contact Lens for 1 year