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Clinical Trial Summary

The purpose of this trial is to evaluate the performance of a new diagnostic device in the diagnosis and management of glaucoma. We will use this new device (PERG) to evaluate the function of the retina in glaucoma patients. This device is safe for the patients.


Clinical Trial Description

Glaucoma is one of the leading causes of blindness worldwide. It's an optic neuropathy characterized by the progressive death of retinal ganglion cells. In laboratories, it's possible to measure the electrical activity of retinal ganglion cells (RGC). Some researchers found that RGC showed electrical anomalies before dying. This decrease of electrical activity can be measured by using pattern electroretinography (PERG). Unfortunately, these measures could not be obtained in clinics before this new device. For this reason, Diopsys developed a new device that can measure PERG directly in clinics, allowing physicians to have these data earlier to help them diagnose pathologies such as glaucoma or other ganglion cells abnormalities. Currently, it is known that glaucoma is difficult to diagnose in the early stages and it's challenging to decide when to start a treatment. In this study, our purpose is to use this new device to evaluate its efficacy in the diagnosis and management of glaucoma. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03330574
Study type Observational
Source Swiss Vision Network
Contact
Status Enrolling by invitation
Phase
Start date January 1, 2017
Completion date December 2023

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