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Visual Performance of Soft Contact Lenses With Myopia Control Optics

NCT05141448 · Status: COMPLETED · Type: INTERVENTIONAL · Enrollment: 79

Last updated 2025-04-27

Study results available
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Summary

This is a multi-site, bilateral, dispensing, randomized, controlled, single-masked, 3x3 crossover study with a run-in period.

Conditions

  • Visual Acuity

Interventions

DEVICE

1-Day Acuvue Moist

Run-in Contact Lens

DEVICE

EMO-118

Test Lens1

DEVICE

EMO-114

Test Lens2

DEVICE

MiSight® 1 day

Control Lens

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
7 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-11-22
Primary Completion
2022-04-01
Completion
2022-04-01

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05141448 on ClinicalTrials.gov