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.
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
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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
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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