Open Lung Maneuvers During High Frequency Oscillatory Ventilation in Preterm Infants (OPEN4HFOV)
Primary Purpose
High Frequency Oscillation Ventilation, Extreme Prematurity, Lung Injury, Acute
Status
Recruiting
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
regular lung recruitment
Sponsored by
About this trial
This is an interventional treatment trial for High Frequency Oscillation Ventilation
Eligibility Criteria
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
Sites / Locations
- Medical University of ViennaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Intervention
Control
Arm Description
lung recruitment maneuvers performed every twelve hours during HFOV
no regular lung recruitment maneuvers during HFOV
Outcomes
Primary Outcome Measures
HFOV oxygen saturation index
oxygen saturation index averaged over high frequency oscillation ventilation for not more than seven consecutive days
Secondary Outcome Measures
bronchopulmonary dysplasia
respiratory support at 36 weeks postmenstrual age
days of ventilation
days on conventional and high frequency oscillation ventilation
overall oxygen saturation index
oxygen saturation index averaged over ventilation time
Full Information
NCT ID
NCT04289324
First Posted
February 25, 2020
Last Updated
October 20, 2023
Sponsor
Medical University of Vienna
1. Study Identification
Unique Protocol Identification Number
NCT04289324
Brief Title
Open Lung Maneuvers During High Frequency Oscillatory Ventilation in Preterm Infants
Acronym
OPEN4HFOV
Official Title
Open Lung Maneuvers During High Frequency Oscillatory Ventilation in Extremely Preterm Infants - A Single Center Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 25, 2020 (Actual)
Primary Completion Date
March 31, 2024 (Anticipated)
Study Completion Date
June 30, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Vienna
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
High Frequency Oscillation Ventilation, Extreme Prematurity, Lung Injury, Acute
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Single center randomized controlled study
Masking
None (Open Label)
Allocation
Randomized
Enrollment
36 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
lung recruitment maneuvers performed every twelve hours during HFOV
Arm Title
Control
Arm Type
No Intervention
Arm Description
no regular lung recruitment maneuvers during HFOV
Intervention Type
Procedure
Intervention Name(s)
regular lung recruitment
Intervention Description
stepwise oxygenation-guided lung recruitment at regular (twelve hours) intervals during high frequency oscillation ventilation
Primary Outcome Measure Information:
Title
HFOV oxygen saturation index
Description
oxygen saturation index averaged over high frequency oscillation ventilation for not more than seven consecutive days
Time Frame
through study completion, an average 10 weeks
Secondary Outcome Measure Information:
Title
bronchopulmonary dysplasia
Description
respiratory support at 36 weeks postmenstrual age
Time Frame
through study completion, an average 10 weeks
Title
days of ventilation
Description
days on conventional and high frequency oscillation ventilation
Time Frame
through study completion, an average 10 weeks
Title
overall oxygen saturation index
Description
oxygen saturation index averaged over ventilation time
Time Frame
through study completion, an average 10 weeks
10. Eligibility
Sex
All
Maximum Age & Unit of Time
8 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tobias Werther
Phone
+4314040032320
Email
tobias.werther@meduniwien.ac.at
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tobias Werther
Organizational Affiliation
Medical University of Vienna
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University of Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tobias Werther
Phone
014040032320
Email
tobias.werther@meduniwien.ac.at
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
10945393
Citation
Rimensberger PC, Pache JC, McKerlie C, Frndova H, Cox PN. Lung recruitment and lung volume maintenance: a strategy for improving oxygenation and preventing lung injury during both conventional mechanical ventilation and high-frequency oscillation. Intensive Care Med. 2000 Jun;26(6):745-55. doi: 10.1007/s001340051242.
Results Reference
result
PubMed Identifier
10835058
Citation
Rimensberger PC, Beghetti M, Hanquinet S, Berner M. First intention high-frequency oscillation with early lung volume optimization improves pulmonary outcome in very low birth weight infants with respiratory distress syndrome. Pediatrics. 2000 Jun;105(6):1202-8. doi: 10.1542/peds.105.6.1202.
Results Reference
result
PubMed Identifier
16763218
Citation
De Jaegere A, van Veenendaal MB, Michiels A, van Kaam AH. Lung recruitment using oxygenation during open lung high-frequency ventilation in preterm infants. Am J Respir Crit Care Med. 2006 Sep 15;174(6):639-45. doi: 10.1164/rccm.200603-351OC. Epub 2006 Jun 8.
Results Reference
result
PubMed Identifier
19364558
Citation
de Waal K, Evans N, van der Lee J, van Kaam A. Effect of lung recruitment on pulmonary, systemic, and ductal blood flow in preterm infants. J Pediatr. 2009 May;154(5):651-5. doi: 10.1016/j.jpeds.2009.01.012.
Results Reference
result
PubMed Identifier
27745747
Citation
Zannin E, Doni D, Ventura ML, Fedeli T, Rigotti C, Dellaca RL, Tagliabue PE. Relationship between Mean Airways Pressure, Lung Mechanics, and Right Ventricular Output during High-Frequency Oscillatory Ventilation in Infants. J Pediatr. 2017 Jan;180:110-115. doi: 10.1016/j.jpeds.2016.09.015. Epub 2016 Oct 10.
Results Reference
result
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Open Lung Maneuvers During High Frequency Oscillatory Ventilation in Preterm Infants
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