Flow Versus Pressure Controlled Ventilation in Patients With Moderate to Severe Acute Respiratory Distress Syndrome

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

The goal of this clinical trial is to compare flow-controlled ventilation (FCV) and pressure-controlled ventilation (PCV) in patients with moderate to severe acute respiratory distress syndrome on the intensive care unit. The main questions it aims to answer are: * Is the mechanical power during flow-controlled ventilation lower than during pressure-controlled ventilation * To gain more understanding about other physiological effects and potential benefits of flow-controlled ventilation in comparison to pressure-controlled ventilation (o.a. the end-expiratory lung volume and homogeneity of ventilation). Participants will be randomized between two ventilation mode sequences, being 90 minutes of FCV followed by 90 minutes of PCV or vice versa.

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

• 18 years or older

• Provided written informed consent

• Undergoing controlled mechanical ventilation via an endotracheal tube

• Meeting all criteria of the Berlin definition of ARDS

‣ Hypoxic respiratory failure within 1 week of a known clinical insult or new or worsening respiratory symptoms

⁃ Bilateral opacities on X-ray or CT-scan not fully explained by effusions, lobar/lung collapse (atelectasis), or nodules

⁃ Respiratory failure not fully explained by cardiac failure or fluid overload.

⁃ Oxygenation: moderate ARDS P/F ratio between 101-200 mmHg, severe ARDS PF ratio ≤ 100mmHg, both with PEEP ≥ 5 cmH2O.

• Intubated ≤72 hours

Locations
Other Locations
Netherlands
Maasstad Hospital
RECRUITING
Rotterdam
Contact Information
Primary
Julien van Oosten, MD
j.vanoosten@erasmusmc.nl
+31630600232
Backup
Annemijn Jonkman, Dr
a.jonkman@erasmusmc.nl
+31627858466
Time Frame
Start Date: 2023-09-12
Estimated Completion Date: 2026-05
Participants
Target number of participants: 28
Treatments
Experimental: FCV-PCV
90 minutes of flow-controlled ventilation followed by 90 minutes of pressure-controlled ventilation.
Experimental: PCV-FCV
90 minutes of pressure-controlled ventilation followed by 90 minutes of flow-controlled ventilation.
Sponsors
Collaborators: Maasstad Hospital
Leads: Erasmus Medical Center

This content was sourced from clinicaltrials.gov