To Study the Function of the Retina in Glaucoma Patients Using PERG

NCT ID: NCT03330574

Last Updated: 2022-05-05

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 200 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2017-01-01
• Study Completion Date: 2023-12-31

Brief 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.

Detailed 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.

Conditions

Glaucoma

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Variability of the device

We will study the repeatability and reliability of the Diopsys® ERG Vision Testing Systems in normal non-glaucomatous people and in those with suspicion of glaucoma or confirmed glaucoma.

No interventions assigned to this group

Diagnosis and progression of glaucoma

Patients who have a suspicion of glaucoma and patients with confirmed glaucoma will be included. PERG data obtained by the Diopsys® ERG Vision Testing Systems will be analyzed to study the PERG changes in different clinical situations, such as early glaucoma and progression of glaucoma.

No interventions assigned to this group

Effect of medical/surgical intervention

Patients will undergo standard treatment based on their medical history and we will observe the PERG changes induced by these treatments (eye drops, laser or surgery) with the Diopsys® ERG Vision Testing Systems.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• Glaucoma (all types of glaucoma);
• Ocular hypertensive (Suspicion of glaucoma);
• Control Patients (without any suspicion/sign of glaucoma);
• Have given written informed consent, prior to any investigational procedures;
• Aged 18 years of either sex.

Exclusion Criteria

• Patients not able to understand the character of the study
• Participation in other clinical research within the last 4 weeks
• Other diseases that may cause visual field loss or optic disc abnormalities
• Systemic diseases that may affect PERG amplitude such as diabetes, parkinsonism, multiple sclerosis
• Poor best corrected visual acuity outside the limits recommended for the test
• Patients with high myopia (>5D)

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Swiss Vision Network

OTHER

Sponsor Role: lead

Responsible Party

Dr. Kaweh Mansouri

Doctor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Kaweh Mansouri, MD

Role: PRINCIPAL_INVESTIGATOR

Glaucoma Center, Montchoisi Clinic

Locations

Montchoisi Clinic

Lausanne, Canton of Vaud, Switzerland

Countries

Switzerland

Other Identifiers

PERG-01

Identifier Type: -

Identifier Source: org_study_id