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Evaluating Visual Acuity and Initial Fit Performance of Two Soft Contact Lenses

NCT04954833 · Status: COMPLETED · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2025-04-27

Study results available
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Summary

This is a multi-center, randomized, controlled, double-masked, 2x2 cross-over, non-dispensing study to compare visual acuity and lens fit performance.

Conditions

  • Visual Acuity

Interventions

DEVICE

EMO-200

TEST Lens

DEVICE

EMO-118

CONTROL Lens

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2021-06-14
Primary Completion
2021-08-16
Completion
2021-08-16

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 NCT04954833 on ClinicalTrials.gov