Infant Forced Oscillations Technique (iFOT) (iFOT)
Primary Purpose
Respiratory Function Tests, Respiratory Disease, Infant, Newborn, Disease
Status
Unknown status
Phase
Not Applicable
Locations
Greece
Study Type
Interventional
Intervention
FOT measurements in newborns and small infants
Sponsored by
About this trial
This is an interventional diagnostic trial for Respiratory Function Tests
Eligibility Criteria
Inclusion Criteria:
- Newborns cared for in the NICU and well-baby nursery of the University Hospital of Patras, Greece.
- Parental written informed consent.
Exclusion Criteria:
- Major respiratory, cardiovascular or other condition that does not permit FOT measurements at the predetermined time points.
- Any infectious disorder with increased risk of contamination.
- Orofacial anomalies (e.g. genetic syndromes) that do not permit proper application of the face mask.
Sites / Locations
- Neonatal Intensive Care Unit, University Hospital of PatrasRecruiting
- Well-baby nursery, Department of Pediatrics, University Hospital of PatrasRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
FOT measurements
Arm Description
FOT measurements in newborns and small infants
Outcomes
Primary Outcome Measures
Respiratory resistance (Rrs) - Term newborns
Rrs at multiple frequencies (FOT) in term infants
Respiratory resistance (Rrs) - Term newborns
Rrs at multiple frequencies (FOT) in term infants
Respiratory resistance (Rrs) - Term newborns
Rrs at multiple frequencies (FOT) in term infants
Respiratory resistance (Rrs) - Term newborns
Rrs at multiple frequencies (FOT) in term infants
Respiratory reactance (Xrs) - Term newborns
Xrs at multiple frequencies (FOT) in term infants
Respiratory reactance (Xrs) - Term newborns
Xrs at multiple frequencies (FOT) in term infants
Respiratory reactance (Xrs) - Term newborns
Xrs at multiple frequencies (FOT) in term infants
Respiratory reactance (Xrs) - Term newborns
Xrs at multiple frequencies (FOT) in term infants
Respiratory resistance (Rrs) - Preterm newborns
Rrs at multiple frequencies (FOT) in preterm infants
Respiratory resistance (Rrs) - Preterm newborns
Rrs at multiple frequencies (FOT) in preterm infants
Respiratory resistance (Rrs) - Preterm newborns
Rrs at multiple frequencies (FOT) in preterm infants
Respiratory resistance (Rrs) - Preterm newborns
Rrs at multiple frequencies (FOT) in preterm infants
Respiratory resistance (Rrs) - Preterm newborns
Rrs at multiple frequencies (FOT) in preterm infants
Respiratory resistance (Rrs) - Preterm newborns
Rrs at multiple frequencies (FOT) in preterm infants
Respiratory reactance (Xrs) - Preterm newborns
Xrs at multiple frequencies (FOT) in preterm infants
Respiratory reactance (Xrs) - Preterm newborns
Xrs at multiple frequencies (FOT) in preterm infants
Respiratory reactance (Xrs) - Preterm newborns
Xrs at multiple frequencies (FOT) in preterm infants
Respiratory reactance (Xrs) - Preterm newborns
Xrs at multiple frequencies (FOT) in preterm infants
Respiratory reactance (Xrs) - Preterm newborns
Xrs at multiple frequencies (FOT) in preterm infants
Respiratory reactance (Xrs) - Preterm newborns
Xrs at multiple frequencies (FOT) in preterm infants
Respiratory resistance (Rrs) - Infancy
Rrs at multiple frequencies (FOT) during infancy
Respiratory resistance (Rrs) - Infancy
Rrs at multiple frequencies (FOT) during infancy
Respiratory resistance (Rrs) - Infancy
Rrs at multiple frequencies (FOT) during infancy
Respiratory reactance (Xrs) - Infancy
Xrs at multiple frequencies (FOT) during infancy
Respiratory reactance (Xrs) - Infancy
Xrs at multiple frequencies (FOT) during infancy
Respiratory reactance (Xrs) - Infancy
Xrs at multiple frequencies (FOT) during infancy
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04697251
Brief Title
Infant Forced Oscillations Technique (iFOT)
Acronym
iFOT
Official Title
Application of Forced Oscillation Technique in Infancy
Study Type
Interventional
2. Study Status
Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
April 1, 2021 (Actual)
Primary Completion Date
September 2022 (Anticipated)
Study Completion Date
March 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Patras
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
The aim of this study is the implementation of Forced Oscillations Technique (FOT) in newborns and small infants using a novel commercially available device.
The objective is to assess the feasibility of the method, provide normative data for the first months of life and describe short- and long-term changes in neonatal respiratory disorders.
The study population will consist of term and preterm newborns admitted to the Neonatal Intensive Care Unit (NICU) or the Well-Baby Nursery of the University Hospital of Patras, Greece. It is estimated that 200 full-term and 150 preterm newborns will be enrolled during a period of 36 months (March 2021 - September 2022).
Measurements will be performed using the TremoFlo N-100 via a face mask, with the infant in the supine position during natural sleep. At least 3 technically acceptable measurements (duration 10s each) will be obtained, as follows:
Healthy full-term neonates: postnatal days 1, 2, 3 and at discharge
Preterm neonates: NICU admission, postnatal days 1, 2 and 3, and on the first day of each additional gestational week until discharge
All participants will be also measured at the age of 3, 6 and 12 months.
Detailed Description
INTRODUCTION Pulmonary function testing during early infancy requires sophisticated equipment, specialized personnel and proper patient's preparation. As a result, lung function testing in newborns and small infants is limited to few highly specialized centers.
The forced oscillations technique (FOT) uses complex pressure signals generated by an external device at the airway opening. The pressure waves are transmitted through the airway tree during tidal breathing and force the anatomical structures of the respiratory system to oscillate. From subsequent pressure and flow signal analysis, the total resistance (Rrs) and reactance (Xrs) of the respiratory system are calculated. The latter relates mainly to the elastic properties of the lung parenchyma and the inertia of the column of air in the airways. Both Rrs and Xrs depend on the frequency of oscillation; lower frequencies (range 5-10Hz) provide information on the mechanical properties of smaller airways and vice versa. FOT measurements can be performed fast (usually in less than 30 s), at the bedside, and do not require patient's cooperation. Therefore, FOT is being viewed as an attractive and promising pulmonary function technique for young infants and newborns.
To date, the introduction of infant FOT in routine clinical practice has been limited due to lack of suitable devices and normative data. Studies based on in-build FOT equipment have shown that the application of the method in small infants is feasible. A recent study, in which a modified commercially available device (Tremoflo C-100, THORASYS Thoracic Medical Systems Inc. Montreal, Canada) was used, also supports the feasibility of the method.
OBJECTIVE The aim of this study is the implementation of FOT in newborns and small infants using a novel commercially available device (Tremoflo N-100, THORASYS), specifically released for this age range.
Our objectives are: a) to assess the feasibility of the method and the repeatability of FOT measurements in newborns and small infants, b) to provide normative data for the first months of life in relation to various parameters (e.g. gender, age, somatometrics, etc) and, c) to describe short- and long-term and Rrs and Xrs changes in neonatal respiratory disease (e.g. respiratory distress syndrome, bronchopulmonary dysplasia, etc).
METHODS Population The study population will consist of term and preterm newborns admitted to the Neonatal Intensive Care Unit (NICU) or the Well-Baby Nursery of the University Hospital of Patras, Greece. It is estimated that 200 full-term and 150 preterm newborns will be enrolled during a period of 36 months (March 2021 - September 2022).
The parents of all infants will provide written informed consent prior to enrollment. The study has been approved by the Research and Ethics Committee of the hospital (decision no. 451/12.11.2020).
Measurements Measurements will be performed using the TremoFlo N-100, at bedside, with the infant in the supine position during quiet natural sleep. The device will be calibrated daily, according to manufacturer's instructions. After proper cleaning and decontamination, the face mask of the device will be preheated at 37oC (to avoid awakening) and will be placed on infant's face. The duration of each measurement will be predetermined at 10 s. At least 3 technically acceptable measurements will be performed per infant, with 30 s intervals between them. The validity of each measurement will be assessed according to the coherence function (automatically determined by the operating system of the device).
Protocol
FOT measurements will be scheduled according to the target population, as follows:
In healthy full-term neonates, measurements will be obtained on postnatal days 1, 2, 3 and at discharge. Parents will be asked and scheduled to repeat testing at the age of 3, 6 and 12 months.
In preterm neonates without respiratory disease, measurements will be performed on NICU admission, on postnatal days 1, 2 and 3, and on the first day of each additional gestational week until discharge. For example, a preterm neonate with gestational age 331/7, will be measured at 331/7, 332/7, 333/7, 334/7, 34, 35, 36, etc. Parents of preterm newborns will be also asked and scheduled to repeat testing at the age of 3, 6 and 12 months.
In preterm neonates with respiratory distress syndrome (RDS) the measurements will be obtained on NICU admission and at 6 and 12 hours after surfactant administration. Thereafter, the same protocol with preterm neonates without respiratory disease will be applied. In mechanically ventilated infants the measurements will be performed via the endotracheal tube, but only if their clinical condition permits FOT testing. In such cases, the device will be calibrated in advance using an endotracheal tube of the same internal diameter, material and length as that positioned on the neonate.
EXPECTED RESULTS AND BENEFITS The study is expected to confirm the feasibility of FOT in newborns and small infants (in NICU or outpatient settings) and, most important, to reveal a series of technical/practical details that may improve the applicability of the method in clinical practice. Finally, the study will provide normative data for this age range, and will assess Rrs and Xrs changes in various respiratory disorders of the neonatal period and early infancy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Function Tests, Respiratory Disease, Infant, Newborn, Disease
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
350 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
FOT measurements
Arm Type
Other
Arm Description
FOT measurements in newborns and small infants
Intervention Type
Diagnostic Test
Intervention Name(s)
FOT measurements in newborns and small infants
Intervention Description
Measurements will be performed using the device TremoFlo N-100, at bedside, with the infant in the supine position during quiet natural sleep. After proper cleaning and decontamination, the face mask of the device will be preheated at 37oC (to avoid awakening) and will be placed on infant's face. The duration of each measurement will be predetermined at 10 s. At least 3 technically acceptable measurements will be performed per infant, with 30 s intervals between them. The validity of each measurement will be assessed according to the coherence function (automatically determined by the operating system of the device).
Primary Outcome Measure Information:
Title
Respiratory resistance (Rrs) - Term newborns
Description
Rrs at multiple frequencies (FOT) in term infants
Time Frame
Postnatal day 1.
Title
Respiratory resistance (Rrs) - Term newborns
Description
Rrs at multiple frequencies (FOT) in term infants
Time Frame
Postnatal day 2.
Title
Respiratory resistance (Rrs) - Term newborns
Description
Rrs at multiple frequencies (FOT) in term infants
Time Frame
Postnatal day 3.
Title
Respiratory resistance (Rrs) - Term newborns
Description
Rrs at multiple frequencies (FOT) in term infants
Time Frame
On the day of discharge.
Title
Respiratory reactance (Xrs) - Term newborns
Description
Xrs at multiple frequencies (FOT) in term infants
Time Frame
Postnatal day 1.
Title
Respiratory reactance (Xrs) - Term newborns
Description
Xrs at multiple frequencies (FOT) in term infants
Time Frame
Postnatal day 2.
Title
Respiratory reactance (Xrs) - Term newborns
Description
Xrs at multiple frequencies (FOT) in term infants
Time Frame
Postnatal day 3.
Title
Respiratory reactance (Xrs) - Term newborns
Description
Xrs at multiple frequencies (FOT) in term infants
Time Frame
On the day of discharge
Title
Respiratory resistance (Rrs) - Preterm newborns
Description
Rrs at multiple frequencies (FOT) in preterm infants
Time Frame
At NICU admission (within the first 2 hours).
Title
Respiratory resistance (Rrs) - Preterm newborns
Description
Rrs at multiple frequencies (FOT) in preterm infants
Time Frame
Postnatal day 1.
Title
Respiratory resistance (Rrs) - Preterm newborns
Description
Rrs at multiple frequencies (FOT) in preterm infants
Time Frame
Postnatal day 2.
Title
Respiratory resistance (Rrs) - Preterm newborns
Description
Rrs at multiple frequencies (FOT) in preterm infants
Time Frame
Postnatal day 3.
Title
Respiratory resistance (Rrs) - Preterm newborns
Description
Rrs at multiple frequencies (FOT) in preterm infants
Time Frame
On the first day of each additional week until 36 weeks post-conceptional age.
Title
Respiratory resistance (Rrs) - Preterm newborns
Description
Rrs at multiple frequencies (FOT) in preterm infants
Time Frame
On the day of discharge.
Title
Respiratory reactance (Xrs) - Preterm newborns
Description
Xrs at multiple frequencies (FOT) in preterm infants
Time Frame
At NICU admission (within the first 2 hours).
Title
Respiratory reactance (Xrs) - Preterm newborns
Description
Xrs at multiple frequencies (FOT) in preterm infants
Time Frame
On postnatal day 1.
Title
Respiratory reactance (Xrs) - Preterm newborns
Description
Xrs at multiple frequencies (FOT) in preterm infants
Time Frame
On postnatal day 2.
Title
Respiratory reactance (Xrs) - Preterm newborns
Description
Xrs at multiple frequencies (FOT) in preterm infants
Time Frame
On postnatal day 3.
Title
Respiratory reactance (Xrs) - Preterm newborns
Description
Xrs at multiple frequencies (FOT) in preterm infants
Time Frame
On the first day of each additional week until 36 weeks post-conceptional age.
Title
Respiratory reactance (Xrs) - Preterm newborns
Description
Xrs at multiple frequencies (FOT) in preterm infants
Time Frame
On the day of discharge.
Title
Respiratory resistance (Rrs) - Infancy
Description
Rrs at multiple frequencies (FOT) during infancy
Time Frame
At the age of 3 months (+/- 1 week)
Title
Respiratory resistance (Rrs) - Infancy
Description
Rrs at multiple frequencies (FOT) during infancy
Time Frame
At the age of 6 months (+/- 1 week)
Title
Respiratory resistance (Rrs) - Infancy
Description
Rrs at multiple frequencies (FOT) during infancy
Time Frame
At the age of 12 months (+/- 2 weeks)
Title
Respiratory reactance (Xrs) - Infancy
Description
Xrs at multiple frequencies (FOT) during infancy
Time Frame
At the age of 3 months (+/- 1 week)
Title
Respiratory reactance (Xrs) - Infancy
Description
Xrs at multiple frequencies (FOT) during infancy
Time Frame
At the age of 6 months (+/- 1 week)
Title
Respiratory reactance (Xrs) - Infancy
Description
Xrs at multiple frequencies (FOT) during infancy
Time Frame
At the age of 12 months (+/- 2 weeks)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
12 Months
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Newborns cared for in the NICU and well-baby nursery of the University Hospital of Patras, Greece.
Parental written informed consent.
Exclusion Criteria:
Major respiratory, cardiovascular or other condition that does not permit FOT measurements at the predetermined time points.
Any infectious disorder with increased risk of contamination.
Orofacial anomalies (e.g. genetic syndromes) that do not permit proper application of the face mask.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sotirios Fouzas, MD, PhD
Phone
6944510047
Email
sfouzas@upatras.gr
First Name & Middle Initial & Last Name or Official Title & Degree
Gabriel Dimitriou, MD, PhD
Email
gdim@upatras.gr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sotirios Fouzas
Organizational Affiliation
University of Patras
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neonatal Intensive Care Unit, University Hospital of Patras
City
Patras
ZIP/Postal Code
26504
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabriel Dimitriou, MD, PhD
Email
gdim@upatras.gr
First Name & Middle Initial & Last Name & Degree
Sotirios Fouzas, MD, PhD
Phone
6944510047
Email
sfouzas@upatras.gr
Facility Name
Well-baby nursery, Department of Pediatrics, University Hospital of Patras
City
Patras
ZIP/Postal Code
26504
Country
Greece
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gabriel Dimitriou, MD, PhD
Email
gdim@upatras.gr
First Name & Middle Initial & Last Name & Degree
Sotirios Fouzas, MD, PhD
Phone
6944510047
Email
sfouzas@upatras.gr
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
No Ethics Committee approval
Citations:
PubMed Identifier
26777151
Citation
Skylogianni E, Douros K, Anthracopoulos MB, Fouzas S. The Forced Oscillation Technique in Paediatric Respiratory Practice. Paediatr Respir Rev. 2016 Mar;18:46-51. doi: 10.1016/j.prrv.2015.11.001. Epub 2015 Nov 10.
Results Reference
background
PubMed Identifier
25154334
Citation
Hantos Z, Czovek D, Gyurkovits Z, Szabo H, Maar BA, Radics B, Virag K, Makan G, Orvos H, Gingl Z, Sly PD. Assessment of respiratory mechanics with forced oscillations in healthy newborns. Pediatr Pulmonol. 2015 Apr;50(4):344-52. doi: 10.1002/ppul.23103. Epub 2014 Aug 25.
Results Reference
background
PubMed Identifier
30464010
Citation
Gray DM, Czovek D, McMillan L, Turkovic L, Stadler JAM, Vanker A, Radics BL, Gingl Z, Hall GL, Sly PD, Zar HJ, Hantos Z. Intra-breath measures of respiratory mechanics in healthy African infants detect risk of respiratory illness in early life. Eur Respir J. 2019 Jan 31;53(2):1800998. doi: 10.1183/13993003.00998-2018. Print 2019 Feb.
Results Reference
background
PubMed Identifier
31935746
Citation
Klinger AP, Travers CP, Martin A, Kuo HC, Alishlash AS, Harris WT, Carlo WA, Ambalavanan N. Non-invasive forced oscillometry to quantify respiratory mechanics in term neonates. Pediatr Res. 2020 Aug;88(2):293-299. doi: 10.1038/s41390-020-0751-7. Epub 2020 Jan 14.
Results Reference
background
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Infant Forced Oscillations Technique (iFOT)
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