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Acute Respiratory Distress SyndromeNCT06051188

FCV vs PCV in Moderate to Severe ARDS

A study of Acute Respiratory Distress Syndrome and Ventilator Lung, run by Erasmus Medical Center at 2 sites in Netherlands.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

The goal of this clinical trial is to compare flow-controlled ventilation (FCV) and pressure-controlled ventilation (PCV) in patients with moderate to severe acute respiratory distress syndrome on the intensive care unit. Read more about this study

Who is it for?
Ages 18 years and older
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
15 participants
Where
2 sitesNetherlands
Study dates
12 Sep 2023to 27 Nov 2025
Phase
Interventional
Are there results?
None posted in the registry

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 years and older
  • 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
  • Meeting all criteria of the Berlin definition of ARDS
  • Hypoxic respiratory failure within 1 week of a known clinical insult or new or worsening respiratory symptoms
  • Bilateral opacities on X-ray or CT-scan not fully explained by effusions, lobar/lung collapse (atelectasis), or nodules
Show all 9Show fewer
  • Respiratory failure not fully explained by cardiac failure or fluid overload.
  • Oxygenation: moderate ARDS P/F ratio between 101-200 mmHg, severe ARDS PF ratio ≤ 100mmHg, both with PEEP ≥ 5 cmH2O.
  • 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
  • Intubated > 72 hours
Show all 18Show fewer
  • Anticipating withdrawal of life support and/or shift to palliation as the goal of care
  • 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.

Netherlands2 sites
  • Maasstad Hospital

    Rotterdam, South Holland, 3079DZ

  • Erasmus Medical Center

    Rotterdam, 3015 GD

Other trials in Netherlands

About this study

Official title: Flow Versus Pressure Controlled Ventilation in Patients With Moderate to Severe Acute Respiratory Distress Syndrome

The goal of this clinical trial is to compare flow-controlled ventilation (FCV) and pressure-controlled ventilation (PCV) in patients with moderate to severe acute respiratory distress syndrome on the intensive care unit.

The main questions it aims to answer are:

Read more
  • Is the mechanical power during flow-controlled ventilation lower than during pressure-controlled ventilation
  • To gain more understanding about other physiological effects and potential benefits of flow-controlled ventilation in comparison to pressure-controlled ventilation (o.a. the end-expiratory lung volume and homogeneity of ventilation).

Participants will be randomized between two ventilation mode sequences, being 90 minutes of FCV followed by 90 minutes of PCV or vice versa.

Read the detailed description

Rationale: During controlled mechanical ventilation (CMV) only the inspiration is controlled by either a set driving pressure (Pressure Controlled Ventilation, PCV) or tidal volume (Volume Controlled Ventilation, VCV). The expiration depends on the passive elastic recoil of the respiratory system and cannot be controlled and lasts until the airway pressure is equal to the positive end-expiratory pressure (PEEP). The exponential decrease in airway pressure during expiration may result in alveolar collapse and hypoxemia. Flow controlled ventilation (FCV) is a mechanical ventilation method that uses a constant flow during both inspiration and expiration. FCV results in a gradual decrease in airway pressure during expiration as flow is controlled. In both animal and prospective crossover studies, controlled expiration resulted in higher mean airway pressures with reduced alveolar collapse. Besides, FCV resulted in a higher ventilation efficiency measured by a decrease in minute volume at stable arterial partial pressures of carbon dioxide (PaCO2). Where a reduction in alveolar collapse may lead to less atelectrauma, a higher ventilation efficiency may lead to a lower mechanical power (MP), which is the amount of energy (Joules) that is transferred to the respiratory system by the mechanical ventilator every minute. Both are important determinants of Ventilator Induced Lung Injury (VILI). This makes FCV a very interesting ventilation mode in patients with the acute respiratory distress syndrome (ARDS) in which VILI is still a major contributor to overall morbidity and mortality. Two prior prospective cross-over studies have been performed in (COVID-19) ARDS patients that did show a lower minute volume with FCV compared to PCV or VCV. However, these studies did not take into account assessments of the MP or end-expiratory lung volume (EELV), which is a measurement of lung aeration.

The investigators hypothesize that FCV in patients with moderate to severe ARDS results in a lower MP and an increased EELV compared to standard CMV modes (PCV or VCV).

Objectives: To study the effect of FCV on the MP and the EELV compared to PCV.

Study design: Randomized crossover physiological pilot study comparing FCV and PCV.

Study population: Patients with moderate to severe ARDS ≥ 18 years old receiving CMV.

Intervention: Patients are mechanically ventilated with PCV mode at baseline. Upon inclusion the EIT-belt and an esophageal balloon are placed to assess the EELV and transpulmonary pressures respectively. Besides, participants are randomized between the sequence of ventilation mode, namely 90 minutes of PCV followed by 90 minutes of FCV or 90 minutes of FCV followed by 90 minutes of PCV. When PCV is switched to FCV the same mechanical ventilator settings are used as in the PCV mode. After half an hour on FCV the PEEP, driving pressure and flow of FCV are optimized based on the highest compliance and lowest flow matching with a stable PaCO2 thereby not exceeding lung protective ventilation limits (transpulmonary driving pressure ≤ 12cmH2O and tidal volumes ≤ 8 ml/kg ideal body weight (IBW)). PCV 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 MP after 90 minutes on FCV compared to after 90 minutes of PCV. An important secondary endpoint is the difference in EELV after 30 minutes on FCV compared to after 30 minutes of PCV.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: All participants 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. During optimization of FCV no lung protective ventilation limits will be exceeded. Therefore, overall, the risks of this study are limited.

Being tested
Flow-controlled ventilation
Keywords
Flow-controlled ventilation, ARDS, Electrical Impedance Tomography, Mechanical Power
Medical subject headings
Respiratory Distress Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Flow-controlled ventilationDevice

    Flow-controlled ventilation (FCV)

Study groups in NCT06051188
Study groupRoleWhat they receive
FCV-PCVExperimental90 minutes of flow-controlled ventilation followed by 90 minutes of pressure-controlled ventilation.
Receives: Device: Flow-controlled ventilation
PCV-FCVExperimental90 minutes of pressure-controlled ventilation followed by 90 minutes of flow-controlled ventilation.
Receives: Device: Flow-controlled ventilation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mechanical power

    Difference in mechanical power in J/min after 90 minutes of flow-controlled ventilation and 90 minutes of pressure-controlled ventilation

    Measured: 90 minutes

Secondary outcomes (10)
  1. End-expiratory lung volume

    Difference in end-expiratory lung volume in milliliters after 30 minutes of flow-controlled ventilation and 30 minutes of pressure-controlled ventilation

    Measured: 30 minutes

  2. Dissipated energy

    Difference in dissipated energy in J/L after 90 minutes of flow-controlled ventilation and 90 minutes of pressure-controlled ventilation

    Measured: 90 minutes

  3. Airway pressures

    Difference in airway pressures in cmH2O (PEEP, PEEPtotal, Ppeak, Pplateau, Pdrive) between FCV and PCV

    Measured: 30 and 90 minutes

  4. Transpulmonary pressures

    Difference in transpulmonary pressures in cmH2O (end-inspiratory transpulmonary pressure, end-expiratory transpulmonary pressure and transpulmonary drivepressure) between FCV and PCV

    Measured: 30 and 90 minutes

  5. Minute volume

    Difference in minute volume in L/min between FCV and PCV

    Measured: 30 and 90 minutes

  6. Ventilatory ratio

    Difference in ventilatory ratio between FCV and PCV

    Measured: 30 and 90 minutes

  7. Electrical Impedance Tomography (EIT)

    Difference in EIT measurements between FCV and PCV (o.a. homogeneity of ventilation)

    Measured: 30 and 90 minutes

  8. P/F ratio

    Difference in P/F ratio between FCV and PCV

    Measured: 30 and 90 minutes

  9. Mean arterial pressure

    Difference in mean arterial pressure (mmHg) between FCV and PCV

    Measured: 30 and 90 minutes

  10. Pulserate

    Difference in pulserate (x/min) between FCV and PCV

    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.

  1. First posted22 Sep 2023
  2. Study start12 Sep 2023
  3. Primary completion27 Nov 2025
  4. Study completion27 Nov 2025

Why it stopped: Not able to apply FCV as intended by manufacturer

Resources

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
Treatment
Allocation
Randomised
Intervention model
Crossover
Model description
Randomized crossover physiological pilot study
Masking
None (open label)
Enrolment
15 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06051188
Sponsor's protocol ID
ABR NL83234.078.23
Status last verified
Nov 2025
First submitted
7 Sep 2023
Last updated
22 Jun 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • van Oosten JP, Francovich JE, Weller D, Rietdijk W, Goedendorp N, Somhorst P, den Uil CA, Gommers D, Jonkman AH, Endeman H. Flow-controlled ventilation versus pressure-controlled ventilation in moderate to severe ARDS patients: a randomized crossover physiological study. Intensive Care Med Exp. 2025 Dec 24;13(1):137. doi: 10.1186/s40635-025-00847-4.

    PubMed 41442110

Questions about this trial

What is this clinical trial studying?

A study of Acute Respiratory Distress Syndrome and Ventilator Lung, 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 9 inclusion and 18 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: stopped early, as of the sponsor's last update on 22 Jun 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?

The study was stopped early (reason given: Not able to apply FCV as intended by manufacturer). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Mechanical power (time frame: 90 minutes). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06051188, which also lists 1 linked publication.

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 22 Jun 2026.

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