Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
ID06024993

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

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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

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Antwerp University Hospital (UZA)

Edegem, Antwerp, Belgium, 2650

Actively Recruiting

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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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