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Open Lung Maneuvers During High Frequency Oscillatory Ventilation in Preterm Infants

Open Lung Maneuvers During High Frequency Oscillatory Ventilation in Extremely Preterm Infants - A Single Center Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04289324
Acronym
OPEN4HFOV
Enrollment
36
Registered
2020-02-28
Start date
2020-02-25
Completion date
2025-08-31
Last updated
2026-08-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Extreme Prematurity, High Frequency Oscillation Ventilation, Lung Injury, Acute

Brief summary

To assess whether stepwise oxygenation-guided lung recruitment at regular intervals reduces the oxygen saturation index (OSI = Mean Airway Pressure × Fraction of inspired Oxygen × 100 / peripheral Oxygen Saturation, OSI = MAPxFiO2x100/SpO2) averaged over high frequency oscillation ventilation (HFOV) time in extremely preterm infants.

Detailed description

Background: Open lung maneuvers aim to recruit and stabilize the majority of collapsed alveoli, using oxygenation as an indirect variable for lung volume. The stepwise oxygenation-guided lung recruitment procedure during frequency oscillatory ventilation (HFOV) in preterm infants has a low risk of lung hyperinflation and air leak syndrome. Nevertheless, open lung maneuvers at regular intervals during HFOV to maintain or restore oxygenation is not implemented as a routine procedure in the neonatal intensive care. Aim of the study: To assess whether stepwise oxygenation-guided lung recruitment at regular intervals reduces the oxygen saturation index (OSI = Mean Airway Pressure × Fraction of inspired Oxygen × 100 / peripheral Oxygen Saturation, OSI = MAPxFiO2x100/SpO2) averaged over HFOV time in extremely preterm infants. Study design: Single center randomized controlled study. Methods: Thirty-six extremely preterm infants below 28 weeks of gestational age and on high frequency oscillation ventilation receive either stepwise oxygenation-guided lung recruitment maneuver at regular intervals (intervention) and upon decision of the care giving team (intervention group) or lung recruitment maneuver only upon decision of the care giving team (standard, control group). The primary outcome is the oxygen saturation index averaged over HFO ventilation time. The observation time of the HFOV will be limited to at most seven days. Sample size: Fifteen infants need to be enrolled in each group to have 80% power (at a two-sided alpha level of 5%) to detect a difference of 25% in the oxygen saturation index between the intervention group and the control group. Main outcome variables: Oxygen saturation index averaged over HFO ventilation time. Secondary outcome variables: Bronchopulmonary dysplasia (BPD); days of ventilation; oxygen saturation index averaged over ventilation time (HFO and conventional ventilation); the following variables measured before, during and after a single stepwise oxygenation-guided recruitment maneuver: echocardiographic parameters, reactance, relative impedance changes, lung ultrasound measurements, transcutaneous partial carbon dioxide (CO2), blood pressure, heart rate.

Interventions

PROCEDUREregular lung recruitment

stepwise oxygenation-guided lung recruitment at regular (twelve hours) intervals during high frequency oscillation ventilation

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Single center randomized controlled study

Eligibility

Sex/Gender
ALL
Age
No minimum to 8 Weeks
Healthy volunteers
No

Inclusion criteria

Preterm infants * born below 28 weeks of gestational age * not older than 29 weeks of postmenstrual age * receive HFOV

Exclusion criteria

* known congenital anomalies of the heart, of the lung, and/or of the central nervous system * known chromosomal abnormalities * participation in other intervention trials

Design outcomes

Primary

MeasureTime frameDescription
HFOV oxygen saturation indexthrough study completion, an average 10 weeksoxygen saturation index averaged over high frequency oscillation ventilation for not more than seven consecutive days

Secondary

MeasureTime frameDescription
bronchopulmonary dysplasiathrough study completion, an average 10 weeksrespiratory support at 36 weeks postmenstrual age
days of ventilationthrough study completion, an average 10 weeksdays on conventional and high frequency oscillation ventilation
overall oxygen saturation indexthrough study completion, an average 10 weeksoxygen saturation index averaged over ventilation time

Countries

Austria

Contacts

PRINCIPAL_INVESTIGATORTobias Werther

Medical University of Vienna

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 7, 2026