Actively Recruiting
Study Comparing Dead Space Ventilation in Mechanical Ventilation Using Flow-Controlled vs Volume-Controlled Methods During Surgery
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
Researchers are investigating differences in dead space ventilation, which is the ventilation of poorly perfused lung areas, during two types of mechanical ventilation: conventional volume-controlled ventilation and a newer flow-controlled ventilation. Dead space ventilation is important because it relates to lung stress and is a predictor of mortality in conditions like acute respiratory distress syndrome. This study focuses on patients undergoing general anesthesia for elective surgery who require mechanical ventilation. Participants will receive two types of ventilation during surgery: 20 minutes of flow-controlled ventilation using the Evone ventilator and 20 minutes of conventional volume-controlled ventilation using either the Aisys CS3 or Flow-i ventilators. Both ventilation modes involve controlled mechanical ventilation while the patient lies in a supine position. The study compares the amount of wasted ventilation during these two methods. During the study, participants will be monitored with standard care devices including arterial and central venous lines and an endotracheal tube. Researchers will measure changes in dead space ventilation over 20 minutes for each ventilation type. The study assesses ventilation efficiency and safety over the course of surgery, with mechanical ventilation expected to last at least 60 minutes. Data collected will help understand how different ventilation methods affect lung function during surgery.
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
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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
J
Joke De Wachter
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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