Retinal Vein Occlusion and Obstructive Sleep Apnea: A Case Control Study

Centre Hospitalier Régional d'Orléans

Overview

This study purpose is to evaluate the association between Retinal Vein Occlusion and Obstructive Sleep Apnea.

There will be two groups of 50 patients. One with Retinal Vein Occlusion, and the other one, with no Retinal Vein Occlusion will be chosen from the consultation. The compared group will be paired on different criteria including hypertension, ocular hypertension, diabetes, sex, age. They will all spend a night at home with a Sleeping Monitor (Nox T3) in order to evaluate if they have an Obstructive Sleep Apnea.

Study Type

INTERVENTIONAL

Allocation

NON_RANDOMIZED

Purpose

PREVENTION

Masking

NONE

Conditions

Retinal Vein Occlusion Obstructive Sleep Apnea

Interventions

Sleeping MonitorOTHER

to evaluate obstructive sleep apnea

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * All patients with an Retinal Vein Occlusion for one group (patients) * All patients with no Retinal Vein Occlusion for the other group (control) Non-inclusion Criteria: * minor * Severe Insomnia * Neuromuscular Disease with respiratory muscle impairment * Chronic opioid medication * Pregnancy women. * Patient under guardianship

Locations (1)

CHR d'Orléans

Orléans, France

Outcomes

Primary Outcomes

Apnea Hypopnea index >5/hour

Obstructive Sleepin Apnea diagnostic depends only on the AHI which is measured by the Sleeping Monitor at home.

Time frame: Hour 12

Secondary Outcomes

Berlin Questionnaire sleep test

High Risk of Sleep Apnea Syndrome: If there are 2 or more Categories where the score is 2 or above Low Risk of Sleep Apnea Syndrome: If there is only 1 or no Categories where the score is 2 or above

Time frame: Hour 12

Data from ClinicalTrials.gov

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