Acute Respiratory Distress Syndrome (ARDS) Clinical Trials

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Personalized Tidal Volume According to Cardiopulmonary Interactions in ARDS

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Treatment of acute respiratory distress syndrome (ARDS) relies on invasive mechanical ventilation with supposedly protective settings (low tidal volume ventilation). Mortality of ARDS remains high in observational studies (40 to 50%). Approximately 30% of ARDS patients exhibit tidal hyperinflation despite low tidal volume ventilation, suggesting that personalization of tidal volume is required to improve ARDS prognostic. To date, reliable bedside tools to adjust tidal volume are lacking. Excessive tidal volume can be detected using computed tomography by quantification of tidal hyperinflation, but this technique is reserved to research studies and requires patient transport to imaging facility. Mechanical ventilation generates cardio-pulmonary interaction, whose magnitude is influenced by tidal volume and respiratory system characteristics. Pulse pressure variation is a bedside tool with potential to quantify cardio-pulmonary interactions. Increasing tidal volume will decrease right ventricular preload and increase right ventricular afterload, hence maximizing cardio-pulmonary interactions. The investigators hypothesize that pulse pressure variation might help to detect excessive tidal volume during a tidal volume challenge (i.e. stepwise increase in tidal volume)

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

• Age greater then 18 years old

• ARDS according to the BERLIN definition with PaO2/FiO2 ratio ≤ 150 mm Hg

• invasive mechanical ventilation in volume controlled mode with tidal volume set to 6 ml/kg predicted body weight

• use of sedation and neuromuscular-blocking agents

• arterial catheter allowing computation of pulse contour cardiac output calibrated with thermodilution

• central venous catheter implanted in the superior vena cava territory

• esophageal balloon

• Computed tomography planned by attending physician

Locations
Other Locations
France
Hospices Civils de Lyon - Hôpital de la Croix Rousse - Service de Médecine Intensive Réanimation
RECRUITING
Lyon
Contact Information
Primary
Jean-Christophe RICHARD
j-christophe.richard@chu-lyon.fr
+33 426109272
Backup
William DANJOU
william.danjou@chu-lyon.fr
+33 472071762
Time Frame
Start Date: 2022-12-29
Estimated Completion Date: 2026-12
Participants
Target number of participants: 10
Treatments
Active_comparator: Standardized tidal volume
Ventilation with tidal volume 6 ml/kg
Experimental: Personalized tidal volume
Ventilation with tidal volume aiming to minimize cardiopulmonary interactions as assessed by pulse pressure variation
Sponsors
Leads: Hospices Civils de Lyon

This content was sourced from clinicaltrials.gov