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Clinical Investigation for a Multifunction Ophthalmic Measurement Device

NCT06565091 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 378

Last updated 2024-08-21

No results posted yet for this study

Summary

The purpose of this clinical investigation is to evaluate the clinical utility of a multifunctional measuring device for Ophtalmology.

The results of this clinical investigation will be used to refine and validate the device design.

378 participants total will be included in the trial, each having only one visit at the investigation center.

Conditions

  • Accommodation Disorder
  • Keratoconus
  • Dry Eye
  • Refractive Errors
  • Accommodative Fatigue
  • Accommodative Inertia
  • Aberration, Corneal Wavefront

Interventions

DEVICE

Measurements of physiological parameters of the anterior chamber

Acquisition by the investigational device

DEVICE

Measurements of the Axial biometry

Acquisition by the investigational device

Sponsors & Collaborators

  • Essilor International

    lead INDUSTRY

Principal Investigators

  • François LE GUYADER, Dr · WEST OPHTA

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
4 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-06-10
Primary Completion
2025-08-31
Completion
2025-08-31

Countries

  • France

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 NCT06565091 on ClinicalTrials.gov