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Clinical Trial Summary

The objective is to compare the refractive parameters of the photorefraction prototype device without cycloplegia with the refractive parameters of reference device, an autorefractometer with and without cycloplegia.


Clinical Trial Description

A single visit will be necessary. After informed consent, and checking of the inclusion and exclusion criteria, investigators will perform measurements with an autorefractometer and with the photorefraction prototype device without cycloplegia followed by an objective refraction with an autorefractometer under cyclopegia. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06295536
Study type Interventional
Source Essilor International
Contact Julien Andoche
Phone +330633602300
Email andochej@essilor.fr
Status Not yet recruiting
Phase N/A
Start date March 2024
Completion date August 2024

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