Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Obstructive Sleep Apnea
  • Retinal Vein Occlusion
Type
Interventional
Phase
Not Applicable
Design
Allocation: Non-RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: case-control comparison studyMasking: None (Open Label)Primary Purpose: Prevention

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

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 spe...

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.

Tracking Information

NCT #
NCT04011358
Collaborators
Not Provided
Investigators
Principal Investigator: Pierre BONICEL, Dr CHR Orléans