Acute Respiratory Distress Syndrome (ARDS) Clinical Trials

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Awake Prone Positioning of Patients Suffering Community Acquired Pneumonia Requiring Nasal High Flow Therapy, Excluding COVID-19

Status: Recruiting
Location: See all (38) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Community acquired pneumonia, in particular when requiring oxygen therapy because of acute hypoxemic respiratory failure and meeting acute respiratory distress syndrome (ARDS) criteria frequently leads to tracheal intubation and poor outcome. Among invasively mechanically ventilated patients with ARDS and presenting a PaO2/FiO2 ratio (arterial partial pressure of oxygen to inspired fraction of oxygen) of less than 150 mmHg, the prone position significantly reduces mortality and represents standard care (Guérin 2013). Among non-intubated COVID-19 patients, a subtype of viral community acquired pneumonia, a recent study showed that awake prone positioning reduces the composite outcome of intubation or death among patients requiring nasal high flow therapy. Furthermore, it favored weaning of nasal high flow therapy. Prone position in patients with non-COVID ARDS treated with high nasal flow was evaluated in 20 patients with predominantly viral pneumonia (Ding 2020) and was associated with improved oxygenation. Coordinating investigator hypothesize that prone positioning of patients suffering non-COVID community acquired pneumonia and undergoing nasal high flow therapy can significantly improve outcome by reducing the need for intubation and associated therapies such as sedation and muscle relaxation.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Adult patients admitted to an intensive care unit or intermediate care unit

• Suspicion of community acquired pneumonia (at least one of the 3 criteria): fever, cough, purulent expectoration

• And abnormalities suggestive of pneumonia by chest X-ray or CT-scan

• PaO2/FiO2 ratio \<300 mmHg (or equivalent SpO2/FiO2 i.e. \< 315 mmHg) under a minimum gas flow of 30 L/min.

• Person affiliated to a French social security system or equivalent

• Informed consent.

Locations
Other Locations
France
Intensive care, University Hospital, Amiens
NOT_YET_RECRUITING
Amiens
Intensive care, University Hospital, Angers
NOT_YET_RECRUITING
Angers
Intensive care, University Hospital, Argenteuil
NOT_YET_RECRUITING
Argenteuil
Intensive care, University Hospital, Belfort
NOT_YET_RECRUITING
Belfort
Intensive care, University Hospital, Besancon
NOT_YET_RECRUITING
Besançon
Intensive care, University Hospital, Bethune
NOT_YET_RECRUITING
Béthune
Intensive care, University Hospital, Blois
NOT_YET_RECRUITING
Blois
Intensive care, University Hospital, Bordeaux
NOT_YET_RECRUITING
Bordeaux
Intensive care, University Hospital, Bourg en Bresse
NOT_YET_RECRUITING
Bourg-en-bresse
Intensive care, University Hospital, Bourges
RECRUITING
Bourges
Intensive care, University Hospital, Brest
NOT_YET_RECRUITING
Brest
Intensive care, University Hospital, Colombes
NOT_YET_RECRUITING
Colombes
Intensive care, University Hospital, Dieppe
NOT_YET_RECRUITING
Dieppe
Intensive care, University Hospital, Dijon
RECRUITING
Dijon
Intensive care, University Hospital, Dreux
NOT_YET_RECRUITING
Dreux
Intensive care, University Hospital, Garches
NOT_YET_RECRUITING
Garche
Intensive care, University Hospital, Grenoble
NOT_YET_RECRUITING
Grenoble
Intensive care, University Hospital, La Roche sur Yon
RECRUITING
La Roche-sur-yon
Intensive care, University Hospital, Le Mans
RECRUITING
Le Mans
Intensive care, University Hospital, Lens
RECRUITING
Lens
Intensive care, University Hospital, Lille
NOT_YET_RECRUITING
Lille
Intensive care, University Hospital, Lorient
NOT_YET_RECRUITING
Lorient
Intensive care, University Hospital, Lyon
NOT_YET_RECRUITING
Lyon
Intensive care, University Hospital, Lyon
NOT_YET_RECRUITING
Lyon
Intensive care, University Hospital, Morlaix
RECRUITING
Morlaix
Intensive care, University Hospital, Nantes
RECRUITING
Nantes
Intensive care, University Hospital, Nice
NOT_YET_RECRUITING
Nice
Intensive care, University Hospital, Nice
NOT_YET_RECRUITING
Nice
Intensive care, University Hospital, Orléans
NOT_YET_RECRUITING
Orléans
Intensive care, University Hospital, Cochin
NOT_YET_RECRUITING
Paris
Intensive care, University Hospital, Tenon
NOT_YET_RECRUITING
Paris
Intensive care, University Hospital, Poitiers
RECRUITING
Poitiers
Intensive care, University Hospital, Rouen
NOT_YET_RECRUITING
Rouen
Intensive care, University Hospital, Saint Brieuc
RECRUITING
Saint-brieuc
Intensive care, University Hospital, Saint Nazaire
RECRUITING
Saint-nazaire
Intensive care, University Hospital, Strasbourg
NOT_YET_RECRUITING
Strasbourg
Intensive care, University Hospital, Strasbourg
NOT_YET_RECRUITING
Strasbourg
Intensive care, University Hospital, Tours
RECRUITING
Tours
Contact Information
Primary
Stephan EHRMANN
stephanehrmann@gmail.com
2.47.47.38.55
Time Frame
Start Date: 2025-11-30
Estimated Completion Date: 2034-10
Participants
Target number of participants: 1078
Treatments
Experimental: Prone position group
patients will be invited and assisted to prone as long as possible every day. The goal is to achieve at least 8h in the prone position per 24h period, with 3-6 prone sessions.
No_intervention: Control group
Usual care including nasal high flow therapy adapted for a SpO2 of 92-95%. No prone positioning.
Sponsors
Leads: University Hospital, Tours

This content was sourced from clinicaltrials.gov