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Terminated Phase 3 Interventional

Microdosed Atropine 0.1% and 0.01% Ophthalmic Solutions for Reduction of Pediatric Myopia Progression

ClinicalTrials.gov ID: NCT03942419

Public ClinicalTrials.gov record NCT03942419. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 5:47 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Double-Masked, Randomized, Placebo-Controlled Phase 3 Study of the Safety and Efficacy of Atropine 0.1% and 0.01% Ophthalmic Solutions Administered With a Microdose Dispenser for the Reduction of Pediatric Myopia Progression (The CHAPERONE Study)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study evaluates the progression of myopia in participants using microdosed atropine 0.01%, atropine 0.1%, or placebo ophthalmic solution. Eligible subjects will administer study medication daily in each eye for 48 months. Efficacy and safety assessments will be performed at visits scheduled for 1, 6, 12, 18, 24, 30 and 36 months after initiation of medication use. Subjects will be re-randomized at the 36 month visit, then followed at 6 month intervals for an additional year.

Study identification

NCT ID
NCT03942419
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eyenovia Inc.
Industry
Enrollment
438 participants

Conditions and interventions

Eligibility (public fields only)

Age range
3 Years to 12 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2, 2019
Primary completion
Oct 30, 2024
Completion
Nov 19, 2024
Last update posted
Jan 5, 2025

2019 – 2024

United States locations

U.S. sites
18
U.S. states
10
U.S. cities
18
Facility City State ZIP Site status
University of Alabama at Birmingham School of Optometry Birmingham Alabama 35294
Midwestern University Glendale Arizona 85308
Canyon City Eyecare Azusa California 91702
UC Berkeley Berkeley California 94720
Marshall Ketchum University College of Optometry Los Angeles California 90037
Ratner Children's Eye Center San Diego California 92093
Illinois College of Optometry Chicago Illinois 60616
Midwestern University Downers Grove Illinois 60515
SUNY College of Optometry New York New York 10036
Wake Forest Health Network Ophthalmology - Oak Hollow High Point North Carolina 27262
Oculus Research Raleigh North Carolina 27603
The Ohio State University - College of Optometry Columbus Ohio 43210
Scott & Christie and Associates Cranberry Township Pennsylvania 16066
Salus University - The Eye Institute Philadelphia Pennsylvania 19141
Primary Eyecare Group Brentwood Tennessee 37027
Southern College of Optometry Memphis Tennessee 38104
Vanderbilt University Medical Center Nashville Tennessee 37232
Virginia Pediatric Eye Center Virginia Beach Virginia 23452

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03942419, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 5, 2025 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03942419 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →