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

Centre Hospitalier Régional d'Orléans

Status: Withdrawn

Conditions: Retinal Vein Occlusion; Obstructive Sleep Apnea

Treatments: Other: Sleeping Monitor

Study type: Interventional

Funder types: Other

Identifiers

NCT04011358

CHRO-2018-14

Details and patient eligibility

About

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

Full description

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.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

Primary purpose: Prevention

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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0 participants in 2 patient groups

Patient

Other group

Description:

Patient with Retinal Vein Occlusion

Treatment:

Other: Sleeping Monitor

Patient control

Other group

Description:

Patient with no Retinal Vein Occlusion

Treatment:

Other: Sleeping Monitor