Obstructive Pulmonary DiseaseNCT06563544
FCV vs VCV in Obstructive and Asthmatic Patients
A study testing FCV in people with Obstructive Pulmonary Disease and Mechanical Ventilation Pressure High, run by Erasmus Medical Center at 2 sites in Netherlands.
Trial summary
The goal of this physiological pilot study with a randomized crossover design is to study the effect of Flow-controlled ventilation (FCV) on the minute volume compared to Volume-controlled ventilation (VCV) in intubated patients with an exacerbation of their asthma or COPD. Read more about this study
- Who is it for?
- Ages 18 to 100 years
- Conditions the study is for
- Obstructive Pulmonary Disease, Mechanical Ventilation Pressure High, Asthma COPD
- What is being tested?
- FCV
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 10 participants
- Where
- 2 sitesNetherlands
- Study dates
- 17 Jan 2025to Oct 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 100 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 18 years or older;
- Provided written informed consent;
- Undergoing controlled mechanical ventilation via an endotracheal tube;
- Reason for intubation being exacerbation of asthma or COPD;
- Intubated ≤72 hours
Who cannot join
- Severe sputum stasis or production requiring frequent bronchial suctioning (more than 5 times per nurse shift)
- Untreated pneumothorax (i.e. no pleural drainage)
- Hemodynamic instability defined as a mean arterial pressure below 60mmHg not responding to fluids and/or vasopressors or a noradrenalin dose >0.5mcrg/kg/min
- High (>15 mmHg) or instable (an increase in sedation or osmotherapy is required) intracranial pressure
- An inner tube diameter of 6mm or less
- Anticipating withdrawal of life support and/or shift to palliation as the goal of care
Show all 17Show fewer
- Inability to perform adequate electrical impedance tomography (EIT) measurements with, e.g.:
- Have a thorax circumference inappropriate for EIT-belt
- Thoracic wounds, bandages or deformities preventing adequate fit of EIT-belt
- Recent (<7 days) pulmonary surgery including pneumonectomy, lobectomy or lung transplantation
- ICD device present (potential interference with proper functioning of the EIT device and ICD device)
- Excessive subcutaneous emphysema
- Contra-indications for nasogastric tube or inability to perform adequate transpulmonary pressure measurements with, e.g.:
- Recent esophageal surgery
- Prior esophagectomy
- Known presence of esophageal varices
- Severe bleeding disorders
Trial locations and contacts
2 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Netherlands2 sites, 2 recruiting
- Recruiting
Erasmus Medical Center
Rotterdam, South Holland, 3015 GD
Gommers, Professor, 0031107035142, d.gommers@erasmusmc.nl
Julien van Oosten, MD
- Recruiting
Maasstad Hospital
Rotterdam, South Holland, 3079DZ
Dolf Weller, +31615051120, wellerd@maasstadziekenhuis.nl
Corstiaan den Uil, Dr.
About this study
Official title: Flow Versus Volume-Controlled Ventilation in Intubated Obstructive and Asthmatic Patients
The goal of this physiological pilot study with a randomized crossover design is to study the effect of Flow-controlled ventilation (FCV) on the minute volume compared to Volume-controlled ventilation (VCV) in intubated patients with an exacerbation of their asthma or COPD.
Our hypothesis is that FCV will results in a lower minute volume compared to VCV in this patient category.
Patients will be randomized between two ventilation sequences, namely 90 minutes of FCV followed by 90 minutes of VCV or vice versa.
Read the detailed description
Rationale: Patients with an exacerbation of asthma or chronic obstructive pulmonary disease (COPD) requiring controlled mechanical ventilation (CMV) on the intensive care unit (ICU) have a mortality rate between 10 and 20%. This mortality rate is largely explained by major complications associated with mechanical ventilation e.g., pneumothorax, cardiovascular collapse and pneumonia. Complications are the result of dynamic hyperinflation that forms the cornerstone in the pathophysiology of both diseases. The diameter of the smaller airways decreases because of inflammation, bronchospasm, mucus (asthma) and the loss of elastic recoil by emphysema (COPD). This leads in particular to a high airway resistance during expiration and the residue of tidal volume in the lung when the next inspiration begins. The result is dynamic hyperinflation with a continuously increasing lung volume with high pressures, pneumothorax (barotrauma) and hemodynamic collapse as a result. During CMV (pressure- or volume controlled ventilation; PCV or VCV) only the inspiration is controlled while expiration is passive, possibly leading to airway collapse and further dynamic hyperinflation. Besides, both ventilation modes are accompanied by high flow rates leading to a further increase in airway resistance and ventilation pressures. Flow controlled ventilation (FCV) is a mechanical ventilation method that uses a relatively low and constant flow during both inspiration and expiration, thereby decreasing airway resistance and preventing airway collapse during expiration. Besides, FCV has shown to have a higher ventilation efficiency measured by a decrease in minute volume at stable arterial partial pressures of carbon dioxide (PaCO2). This makes FCV a very interesting ventilation mode in intubated patients with an exacerbation of asthma or COPD, possibly decreasing the amount of dynamic hyperinflation and complications in these patients. Although FCV is widely used for hypoxic respiratory failure on the ICU so far no studies have been performed in asthma or COPD patients.
We hypothesize that FCV in intubated patients with an exacerbation of asthma or COPD results in a lower minute volume (MV) and decreased end-inspiratory lung volume (EILV) as a measurement for dynamic hyperinflation compared to VCV.
Objectives: To study the effect of FCV on the MV and EILV compared to VCV.
Study design: Physiological pilot study with a randomized crossover design comparing FCV and VCV.
Study population: Patients with an asthma/COPD exacerbation ≥18 years old receiving CMV.
Intervention: Patients are mechanically ventilated with VCV at baseline. Upon inclusion the EIT-belt and an esophageal balloon are placed to assess the EILV and transpulmonary pressures respectively. Besides, patients are randomized between the sequence of ventilation mode, namely 90 minutes of VCV followed by 90 minutes of FCV or 90 minutes of FCV followed by 90 minutes of VCV. When VCV is switched to FCV the same mechanical ventilator settings are used as in the VCV mode. After half an hour on FCV the PEEP, drivingpressure and flow of FCV are optimized based on the highest compliance and lowest flow matching with a stable PaCO2. VCV is always set according to standard of care. Total time of measurements / study time is 180 minutes.
Main study parameters/endpoints: Primary endpoint is the difference in minute volume after 90 minutes on FCV compared to after 90 minutes of VCV. An important secondary endpoint is the difference in EILV after 30 minutes on FCV compared to after 30 minutes of VCV.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: All patients are sedated and on CMV, therefore there will be no discomfort for the patient. FCV has been successfully applied during surgery and on the ICU and the patient will be monitored continuously so the clinical team can act directly in case of any adverse event. Lung volume is measured with EIT, a non-invasive, radiation-free monitoring tool. Transpulmonary pressures are measured with an esophageal balloon that is placed in a similar manor as a nasogastric feeding tube. Therefore, overall the risks of this study are limited.
- Being tested
- FCV
- Medical subject headings
- Lung Diseases, Obstructive
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
FCVDevice
Also called Flow-controlled ventilation
90 minutes of FCV
| Study group | Role | What they receive |
|---|---|---|
| FCV-VCV | Experimental | 90 minutes of FCV followed by 90 minutes of VCV Receives: Device: FCV |
| VCV-FCV | Experimental | 90 minutes of VCV followed by 90 minutes of FCV Receives: Device: FCV |
What is being measured
The primary outcome is the main question the study is designed to answer.
MV
Minute Volume
Measured: 90 minutes
Secondary outcomes (10)
EILV
End-inspiratory lung volume
Measured: 90 minutes
Vei
Volume end-inspiratory
Measured: 90 minutes
MP
Mechanical Power (J/min)
Measured: 90 minutes
Dissipated energy
Measured: 30 and 90 minutes
Airway pressures
(peak airway pressure, plateau pressure, mean airway pressure, PEEP, intrinsic PEEP, driving pressure
Measured: 30 and 90 minutes
Transpulmonary pressures
(end-expiratory transpulmonary pressure, end-inspiratory transpulmonary pressure, transpulmonary driving pressure
Measured: 30 and 90 minutes
RVDI
Regional ventilation delay index
Measured: 30 and 90 minutes
GI
Global Inhomogeneity index
Measured: 30 and 90 minutes
Gas exchange
Arterial blood gas values, ventilatory ratio
Measured: 30 and 90 minutes
Hemodynamic parameters
Pulse rate and mean blood pressure
Measured: 30 and 90 minutes
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Aug 2024
- Study start17 Jan 2025
- Primary completionOct 2026 (estimated)
- Study completionOct 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Obstructive Pulmonary DiseaseStudies of the same condition, open and under way.
- More trials run by Erasmus Medical CenterThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Model description
- Physiological pilot study with a randomized crossover design comparing FCV and VCV
- Masking
- None (open label)
- Enrolment
- 10 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Erasmus Medical Center
- Sponsor type
- University, hospital or other
- Collaborators
- Maasstad Hospital
- Responsible party
- Principal investigator, Annemijn Jonkman, Erasmus Medical Center
- Investigators
- Diederik P Gommers, Prof. Dr., Study director, Erasmus Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06563544
- Sponsor's protocol ID
- ABR NL86078.078.24
- Status last verified
- Aug 2026
- First submitted
- 19 Aug 2024
- Last updated
- 13 Aug 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: After the study is completed the researchers will deliver the study data to other researchers if asked for with good argumentation
Study at a glance
From the registry record, last updated by the sponsor on 13 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Flow Versus Volume-Controlled Ventilation in Intubated Obstructive and Asthmatic Patients
- ClinicalTrials.gov ID
- NCT06563544
- Acronym / sponsor ID
- ABR NL86078.078.24
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 10 participants (estimated)
- Lead sponsor
- Erasmus Medical CenterUniversity, hospital or other
- Collaborators
- Maasstad Hospital
- Study start
- 17 Jan 2025 (actual)
- Primary completion
- Oct 2026 (estimated)
- Study completion
- Oct 2027 (estimated)
- First posted
- 21 Aug 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this physiological pilot study with a randomized crossover design is to study the effect of Flow-controlled ventilation (FCV) on the minute volume compared to Volume-controlled ventilation (VCV) in intubated patients with an exacerbation of their asthma or COPD.
Our hypothesis is that FCV will results in a lower minute volume compared to VCV in this patient category.
Patients will be randomized between two ventilation sequences, namely 90 minutes of FCV followed by 90 minutes of VCV or vice versa.
Detailed description
Rationale: Patients with an exacerbation of asthma or chronic obstructive pulmonary disease (COPD) requiring controlled mechanical ventilation (CMV) on the intensive care unit (ICU) have a mortality rate between 10 and 20%. This mortality rate is largely explained by major complications associated with mechanical ventilation e.g., pneumothorax, cardiovascular collapse and pneumonia. Complications are the result of dynamic hyperinflation that forms the cornerstone in the pathophysiology of both diseases. The diameter of the smaller airways decreases because of inflammation, bronchospasm, mucus (asthma) and the loss of elastic recoil by emphysema (COPD). This leads in particular to a high airway resistance during expiration and the residue of tidal volume in the lung when the next inspiration begins. The result is dynamic hyperinflation with a continuously increasing lung volume with high pressures, pneumothorax (barotrauma) and hemodynamic collapse as a result. During CMV (pressure- or volume controlled ventilation; PCV or VCV) only the inspiration is controlled while expiration is passive, possibly leading to airway collapse and further dynamic hyperinflation. Besides, both ventilation modes are accompanied by high flow rates leading to a further increase in airway resistance and ventilation pressures. Flow controlled ventilation (FCV) is a mechanical ventilation method that uses a relatively low and constant flow during both inspiration and expiration, thereby decreasing airway resistance and preventing airway collapse during expiration. Besides, FCV has shown to have a higher ventilation efficiency measured by a decrease in minute volume at stable arterial partial pressures of carbon dioxide (PaCO2). This makes FCV a very interesting ventilation mode in intubated patients with an exacerbation of asthma or COPD, possibly decreasing the amount of dynamic hyperinflation and complications in these patients. Although FCV is widely used for hypoxic respiratory failure on the ICU so far no studies have been performed in asthma or COPD patients.
We hypothesize that FCV in intubated patients with an exacerbation of asthma or COPD results in a lower minute volume (MV) and decreased end-inspiratory lung volume (EILV) as a measurement for dynamic hyperinflation compared to VCV.
Objectives: To study the effect of FCV on the MV and EILV compared to VCV.
Study design: Physiological pilot study with a randomized crossover design comparing FCV and VCV.
Study population: Patients with an asthma/COPD exacerbation ≥18 years old receiving CMV.
Intervention: Patients are mechanically ventilated with VCV at baseline. Upon inclusion the EIT-belt and an esophageal balloon are placed to assess the EILV and transpulmonary pressures respectively. Besides, patients are randomized between the sequence of ventilation mode, namely 90 minutes of VCV followed by 90 minutes of FCV or 90 minutes of FCV followed by 90 minutes of VCV. When VCV is switched to FCV the same mechanical ventilator settings are used as in the VCV mode. After half an hour on FCV the PEEP, drivingpressure and flow of FCV are optimized based on the highest compliance and lowest flow matching with a stable PaCO2. VCV is always set according to standard of care. Total time of measurements / study time is 180 minutes.
Main study parameters/endpoints: Primary endpoint is the difference in minute volume after 90 minutes on FCV compared to after 90 minutes of VCV. An important secondary endpoint is the difference in EILV after 30 minutes on FCV compared to after 30 minutes of VCV.
Nature and extent of the burden and risks associated with participation, benefit and group relatedness: All patients are sedated and on CMV, therefore there will be no discomfort for the patient. FCV has been successfully applied during surgery and on the ICU and the patient will be monitored continuously so the clinical team can act directly in case of any adverse event. Lung volume is measured with EIT, a non-invasive, radiation-free monitoring tool. Transpulmonary pressures are measured with an esophageal balloon that is placed in a similar manor as a nasogastric feeding tube. Therefore, overall the risks of this study are limited.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- Physiological pilot study with a randomized crossover design comparing FCV and VCV
| Arm | Type | Receives |
|---|---|---|
| FCV-VCV | Experimental | Device: FCV90 minutes of FCV followed by 90 minutes of VCV |
| VCV-FCV | Experimental | Device: FCV90 minutes of VCV followed by 90 minutes of FCV |
Who may qualify
- Ages
- 18 to 100 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- 18 years or older;
- Provided written informed consent;
- Undergoing controlled mechanical ventilation via an endotracheal tube;
- Reason for intubation being exacerbation of asthma or COPD;
- Intubated ≤72 hours
Key exclusion criteria (17 listed)
- Severe sputum stasis or production requiring frequent bronchial suctioning (more than 5 times per nurse shift)
- Untreated pneumothorax (i.e. no pleural drainage)
- Hemodynamic instability defined as a mean arterial pressure below 60mmHg not responding to fluids and/or vasopressors or a noradrenalin dose >0.5mcrg/kg/min
- High (>15 mmHg) or instable (an increase in sedation or osmotherapy is required) intracranial pressure
- An inner tube diameter of 6mm or less
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| FCVAlso: Flow-controlled ventilation90 minutes of FCV | Device | FCV-VCV, VCV-FCV |
Primary outcome
MV
Time frame: 90 minutes
Minute Volume
10 secondary outcomes
EILV
Time frame: 90 minutes
Vei
Time frame: 90 minutes
MP
Time frame: 90 minutes
Dissipated energy
Time frame: 30 and 90 minutes
Airway pressures
Time frame: 30 and 90 minutes
Transpulmonary pressures
Time frame: 30 and 90 minutes
RVDI
Time frame: 30 and 90 minutes
GI
Time frame: 30 and 90 minutes
Gas exchange
Time frame: 30 and 90 minutes
Hemodynamic parameters
Time frame: 30 and 90 minutes
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Aug 2026.
- Individual participant dataSharing planned: Yes. After the study is completed the researchers will deliver the study data to other researchers if asked for with good argumentation
Related trials for Obstructive Pulmonary Disease
RecruitingPhase 1
Serial Amnioinfusions as Regenerative Therapy for Pulmonary Hypoplasia
Renal Failure Congenital, Congenital Renal Anomaly Nos
Active, not recruiting
Symptoms and Functions in Patients With COPD and Chronic Bronchitis Switching From CIG to THS
COPD, Smoking
RecruitingPhase 1
Pilot Study to Identify the Mediators and Inflammatory Cell Surface Receptors Involved in Allergic Airway Inflammation
Asthma
Not yet recruitingPhase 2/3
An Open-Label Extension Study to Evaluate Inhaled Treprostinil SMI in Participants With Pulmonary Hypertension Associated With Chronic Obstructive Pulmonary Disease (PH-COPD)
Pulmonary Hypertension Associated With Chronic Obstructive Pulmonary Disease
Not yet recruiting
The Aim of the Study is to Decipher the Alterations in Signalling Pathways of Skeletal Muscle Stem Cells (Satellite Cells (SCs)) in Individuals With COPD, as Well as to Examine the Effect of Exercise Training on SCs.
COPD (Chronic Obstructive Pulmonary Disease), Sarcopenia in Elderly
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Diederik P Gommers, Prof. Dr. study director
Erasmus Medical Center
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing FCV in people with Obstructive Pulmonary Disease and Mechanical Ventilation Pressure High, run by Erasmus Medical Center at 2 sites in Netherlands.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 13 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Netherlands. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Julien P Van Oosten, MD (+31630600232, j.vanoosten@erasmusmc.nl), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
MV (time frame: 90 minutes). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Aug 2026.