Closed-loop syncHronization vErsuS convenTional Synchronization in sPontaneously Breathing Adult Nonivasive ventilationPatients

Recruiting N/A Interventional Study
Acute Respiratory Failure Acute Respiratory Distress Syndrome Chronic Respiratory Failure
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
38 (estimated)
Sponsor
Başakşehir Çam & Sakura City Hospital · Government
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About This Trial
The study is a multicentric prospective randomised cross-over study. It evaluates the compatibility of patients with the device without altering the routine treatment applied. During this evaluation, either the clinician-adjusted values on the device or the standard pre-set values are used to obtain hourly and 30-minute PVA (Patient Ventilator Asynchrony) recordings. These recordings will be analy…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adult patients older than 18 years of age * Hospitalized at the ICU or emergency department with the intention of treatment with Noninvasive ventilation at least for the upcoming 2 hours with spontaneous breathing activity * Written informed consent signed and dated by the pat…
Contacts

Ramazan Guven, Associate professor

05324935995

drramazanguven@gmail.com

CONTACT

Tuba Dogan, MD

dr.tubadogan@hotmail.com

CONTACT