Early Verticalization of the Patient With Acute Respiratory Distress Syndrome: Assessment of Feasibility and Safety.

Recruiting N/A Interventional Study
Acute Respiratory Distress Syndrome Prone Position
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
32 (estimated)
Sponsor
Centre Hospitalier Régional d'Orléans · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
Acute Respiratory Distress Syndrome (ARDS) is defined according to the Berlin definition (1) as diffuse lung damage occurring in patients with a predisposing risk factor. Positioning in the prone position (PP) has been shown to decrease mortality in patients with moderate to severe ARDS. However, this technique is not without deleterious effects such as ventilator-associated pneumonia, endotrach…
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Major patient \> 18 years of age * ARDS patients with PaO2/FiO2 ratio \< 150 at any time within 24 hours prior to the screening visit * Hemodynamically stable patient with mean arterial pressure (MAP) \> 65 mmHg maintained without vasopressor or with norepinephrine at a dosage…
Contacts

Aurélie DESPUJOLS

+33238744071

aurelie.despujols@chr-orleans.fr

CONTACT

Elodie POUGOUE TOUKO

+33238744086

elodie.pougoue@chro-orleans.fr

CONTACT