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Evaluating Accommodative Responses of Soft Contact Lenses for Myopia Control

NCT03635528 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 11

Last updated 2020-08-20

No results posted yet for this study

Summary

This is a bilateral, non-dispensing, randomized, controlled, double-masked, 7x7 cross-over study. Each subject will be bilaterally fitted with one of the 7 test articles in each of the 7 periods for a total of four visits. Up to two lens types will be fit at each of the four study visits.

Conditions

  • Visual Acuity

Interventions

DEVICE

Test Lens 1

EMO-114

DEVICE

Test Lens 2

EMO-116

DEVICE

Test Lens 3

EMO-118

DEVICE

Test Lens 4

RMY-100

DEVICE

Test Lens 5

Biofinity multifocal D Lens

DEVICE

Control Lens 1

EMO-117

DEVICE

Control Lens 2

Proclear 1 day

Sponsors & Collaborators

  • Johnson & Johnson Vision Care, Inc.

    lead INDUSTRY

Principal Investigators

  • Xu Cheng · Johnson & Johnson Vision Care, Inc.

Study Design

Allocation
RANDOMIZED
Purpose
DEVICE_FEASIBILITY
Masking
DOUBLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2018-11-29
Primary Completion
2019-07-18
Completion
2019-07-18
FDA Device
Yes

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 NCT03635528 on ClinicalTrials.gov