Actively Recruiting

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

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

17 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 studying mechanical ventilation methods used during surgery, focusing on two types: conventional volume-controlled ventilation (VCV) and flow-controlled ventilation (FCV). FCV is a newer ventilation mode that controls the expiratory flow constantly, unlike conventional ventilation that relies on natural chest recoil. This trial aims to compare the amount of dead space ventilation, or "wasted ventilation," between these two methods, as dead space relates to lung function and patient outcomes during mechanical ventilation. Participants will receive both ventilation methods in a randomized order during surgery under general anesthesia. After setting baseline ventilation with VCV, participants will receive 20 minutes of FCV followed by 20 minutes of VCV, or vice versa. FCV will be delivered using the Evone ventilator, while VCV will use standard ventilators like the Aisys CS3 or Flow-i. This crossover design allows direct comparison of ventilation effects within the same participant. During the trial, researchers will measure various lung function and ventilation parameters, including different types of dead space ventilation, airway pressures, lung volumes, blood gas levels, and cardiac output. These measurements will be taken during each 20-minute ventilation period. Participants are expected to be under general anesthesia with standard monitoring lines in place, and the study will last for the duration of the controlled mechanical ventilation during surgery. Safety and ventilation efficiency will be closely monitored throughout.

CONDITIONS

Brief 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 aged 18 to 70 years
  • Undergoing general anesthesia for elective surgery
  • Have arterial line, central venous line, and endotracheal tube as part of standard care
  • Expected duration of controlled mechanical ventilation of at least 60 minutes
  • Positioned supine (0°±10°) during surgery
Not Eligible

You will not qualify if you...

  • One lung ventilation
  • Known pregnancy
  • Increased intra-abdominal pressure due to pneumoperitoneum or obesity (BMI > 30 kg/m2)
  • Severe COPD (GOLD IV) or dependence on home oxygen
  • Presence of cardiac pacemaker, implantable cardioverter-defibrillator (ICD), or thoracic neurostimulator
  • Skin lesions at the site for Electrical Impedance Tomography (EIT) band placement
  • Signs of raised intracranial pressure
  • Potential interference with surgery due to study equipment setup
  • Patient refusal to participate

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Approximately 60 minutes

Participants undergo two ventilation methods during general anesthesia: 20 minutes of flow-controlled ventilation followed by 20 minutes of conventional volume-controlled ventilation, or vice versa, with baseline ventilation settings titrated beforehand.

1 in-person visit during surgery

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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