Actively Recruiting
Dead Space in Mechanical Ventilation With Constant Expiratory Flow
Led by University Hospital, Antwerp · Updated on 2025-01-22
13
Participants Needed
1
Research Sites
92 weeks
Total Duration
On this page
Sponsors
U
University Hospital, Antwerp
Lead Sponsor
U
Universiteit Antwerpen
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Dead Space in Mechanical Ventilation With Constant Expiratory Flow
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 to 70 years old
- Undergoing general anesthesia for elective surgery
- Have arterial line, central venous line, and endotracheal tube as part of standard care
- Expected to require controlled mechanical ventilation for 60 minutes or more
- Positioned supine (0±10 degrees) during surgery
You will not qualify if you...
- Receiving one-lung ventilation
- Known pregnancy
- Increased intra-abdominal pressure due to pneumoperitoneum or obesity (BMI > 30 kg/m2)
- Severe chronic obstructive pulmonary disease (COPD GOLD IV) or need for home oxygen
- Presence of cardiac pacemaker, implantable cardioverter-defibrillator, or thoracic neurostimulator
- Skin lesions such as injury or inflammation at the site for Electrical Impedance Tomography band application
- Clinical signs of raised intracranial pressure
- Setup of study instruments could interfere with surgery
- Patient refusal to participate
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Antwerp University Hospital (UZA)
Edegem, Antwerp, Belgium, 2650
Actively Recruiting
Research Team
C
Carine Smitz
CONTACT
J
Joke De Wachter
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
BASIC_SCIENCE
Number of Arms
2
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