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Impact of Early Ventilation in Stroke Outcomes in Patients With Sleep Apnea After First Ever Stroke

Stroke Clinical Trial

Official title:
A Single-center, Randomized, Open Label, Parallel Arm, Prospective Study to Evaluate the Impact of Early Ventilation in Stroke Outcomes in Patients With Sleep Apnea After First Ever Stroke

Clinical Trial Summary

To evaluate the impact of early ventilation in stroke outcomes in patients with sleep apnea and first ever stroke, 1 month after stroke.

Clinical Trial Description

Single-center, randomized, open label, parallel arm, prospective study in patients with sleep apnea after first-ever stroke. The study will consist of screening, baseline assessment, interventional period (consisting of a treatment period and follow-up visits), and a follow-up phone call. Patients will be randomly assigned to ASV (active) or control groups, within 4 days after the PSG II and will start the respective intervention in the same day. Patients assigned to the active group will receive ventilatory support with ASV (DreamStation BiPAP autoSV®) during diurnal and nocturnal sleep, from study randomization until clinically indicated. Patients assigned to control group will receive best medical treatment for stroke alone, including rehabilitation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04903951
Study type Interventional
Source Philips Portuguesa S.A.
Contact Sílvia Correia, MD
Phone 00351969043466
Email silviapaiscorreia@gmail.com
Status Not yet recruiting
Phase Phase 2
Start date November 2022
Completion date August 2023
View Details
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