A Clinical Study to Evaluate the Remote Monitoring of Myopia Patients With the EyeQue Insight

NCT04693260 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2022-08-22

No results posted yet for this study

Summary

The objective of this study is to determine whether the remote monitoring of myopia patients with the EyeQue Insight (visual acuity test) can replace regularly scheduled follow-up visits.

Conditions

  • Myopia

Interventions

DEVICE

Visual Acuity with a Hand-held Device Supported by Mobile App.

The Insight will be compared to a standard ETDRS eyechart

Sponsors & Collaborators

  • Eye Boutique Optometry

    collaborator UNKNOWN
  • EyeQue Corp.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
SCREENING
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
7 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-07-03
Primary Completion
2021-09-10
Completion
2021-09-10
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 NCT04693260 on ClinicalTrials.gov