Clinical Trial

Dead Space in Mechanical Ventilation With Constant Expiratory Flow

Study acronym: DeXFLoW
Recruiting
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Record status
This record was last updated January 22, 2025 (before its estimated December 30, 2025 completion). Its status may not reflect the trial's current state.
Summary
Conventional continuous mandatory mechanical ventilation relies on the passive recoil of the chest wall for expiration. This results in an exponentially decreasing expiratory flow. Flow controlled ventilation (FCV), a new ventilation mode with constant, continuous, controlled expiratory flow, has recently become clinically available and is increasingly being adopted for complex mechanical ventilation during surgery. In both clinical and pre-clinical settings, an improvement in ventilation (CO2 clearance) has been observed during FCV compared to conventional ventilation. Recently, Schranc et al. compared flow-controlled ventilation with pressure-regulated volume control in both double lung ventilation and one-lung ventilation in pigs. They report differences in dead space ventilation that may explain the improved CO2 clearance, although their study was not designed to compare dead space ventilation within the group of double lung ventilation. Dead space ventilation, or "wasted ventilation", is the ventilation of hypoperfused lung zones, and is clinically relevant, as it is a strong predictor of mortality in patients with the acute respiratory distress syndrome (ARDS) and is correlated with higher airway driving pressures which are thought to be injurious to the lung (lung stress). This trial aims to study the difference in dead space ventilation between conventional mechanical ventilation in volume-controlled mode and flow controlled-ventilation.
Protocol Amendment History 5 amendments
This ClinicalTrials.gov record has been amended 5 times since 2023-09-05; most recent amendment 2025-01-20.
Status change: Not Yet Recruiting → Recruiting 2025-01-20
Trial Details
NCT Number NCT06024993
Lead Sponsor University Hospital, Antwerp
Collaborators: Universiteit Antwerpen
Conditions Mechanical Ventilation, Artificial Respiration
Enrollment 13 participants
Start Date 2024-07-22
Primary Completion 2025-12-30 (estimated)
Study Completion 2026-04-30 (estimated)
Updated on ClinicalTrials.gov 2025-01-22