Medium vs Low Oxygen Threshold for the Surfactant Administration
Primary Purpose
Respiratory Distress Syndrome
Status
Not yet recruiting
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
Poractant Alfa 80 mg/mL Intratracheal Suspension
Sponsored by
About this trial
This is an interventional treatment trial for Respiratory Distress Syndrome focused on measuring RDS, Surfactant, Threshold, Oxygen, Preterm, Infant
Eligibility Criteria
Inclusion Criteria:
- gestational age less than 32 weeks;
- diagnosis of respiratory distress (RDS);
- need for ventilatory support;
- written informed consent.
Exclusion Criteria:
- congenital malformations;
- genetic disorders;
- perinatal asphyxia.
- neonatal pneumonia or wet lung or meconium aspiration syndrome at birth.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Low FiO2 threshold
Medium FiO2 threshold
Arm Description
A fraction of inspired oxygen (FiO2) of 25% to have an oxygen saturation (SpO2) of 90-92%.
A fraction of inspired oxygen (FiO2) of 35% to have an oxygen saturation (SpO2) of 90-92%.
Outcomes
Primary Outcome Measures
Respiratory pulmonary function
The oxygen saturation (SpO2) to fraction of inspired oxygen (FiO2) ratio (SFR)
Secondary Outcome Measures
Endotracheal intubation
The need of endotracheal intubation after surfactant administration
Oxygen therapy
The need of oxygen therapy
Respiratory Support-1
The need of respiratory support
Respiratory Support-1
Oxygenation index as indicator of the intensity of ventilatory
Respiratory severity-1
Silvermann score as secondary respiratory severity index
Respiratory severity-2
Lung ultrasound score (LUS) score as secondary respiratory severity index
Long-term respiratory pulmonary function
The oxygen saturation (SpO2) to fraction of inspired oxygen (FiO2) ratio (SFR)
Complications of prematurity
The incidence of intraventricular hemorrhage of grade 3-4, periventricular leukomalacia, bronchopulmonary dysplasia, sepsis and retinopathy of prematurity
In-hospital death
death before 36 weeks of gestation
Full Information
NCT ID
NCT04199364
First Posted
December 12, 2019
Last Updated
April 15, 2021
Sponsor
Virgilio Paolo Carnielli
1. Study Identification
Unique Protocol Identification Number
NCT04199364
Brief Title
Medium vs Low Oxygen Threshold for the Surfactant Administration
Official Title
Comparison of Two Fraction Oxygen Inspired (FiO2) Thresholds for the Surfactant Administration in Preterm Infants With Respiratory Disease Syndrome: a Single-center Randomized Phase IV Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2021
Overall Recruitment Status
Not yet recruiting
Study Start Date
June 1, 2021 (Anticipated)
Primary Completion Date
July 1, 2024 (Anticipated)
Study Completion Date
April 30, 2025 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Virgilio Paolo Carnielli
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The aim of this study will be to assess the better fraction inspired oxygen (FiO2) threshold for the surfactant treatment in preterm infants with respiratory distress syndrome (RDS) randomized to receive exogenous surfactant at 25% or 35% of FiO2 threshold. The pulmonary gas-exchanges will be evaluated by oxygen saturation (SpO2) to FiO2 ratio (SFR) and will be used to define the better FiO2 threshold for the surfactant treatment.
Detailed Description
Exogenous surfactant therapy is an effective treatment of neonatal respiratory distress syndrome (RDS) and has been associated with reduced severity of respiratory distress and mortality. The 2019 European guidelines for neonatal RDS treatment suggest as the threshold of inspired oxygen (FiO2) for the surfactant treatment at 30% for all gestational age, but there are no randomized studies that confirm this indication. Some observational studies reported that a relevant number of patients who are not routinely treated with surfactant had respiratory complications, thus they received exogenous surfactant. To date, the optimal FiO2 threshold for surfactant administration remains unclear.
In this single-center, randomized, phase 4 trial, preterm infants (gestational age<32 weeks) with RDS will be randomized to receive exogenous surfactant at 25% or 35% of FiO2 threshold. According to the unit policy, the exogenous surfactant will be administered by an endotracheal tube in intubated infants, or by Intubation-Surfactant-Extubation (InSurE) / Less Invasive Surfactant Administration (LISA) methods in infants who will not remain intubated. The method used for the surfactant administration will be at the discretion of the caring physician.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Distress Syndrome
Keywords
RDS, Surfactant, Threshold, Oxygen, Preterm, Infant
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Masking Description
Participants will be masked.
Allocation
Randomized
Enrollment
200 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Low FiO2 threshold
Arm Type
Experimental
Arm Description
A fraction of inspired oxygen (FiO2) of 25% to have an oxygen saturation (SpO2) of 90-92%.
Arm Title
Medium FiO2 threshold
Arm Type
Experimental
Arm Description
A fraction of inspired oxygen (FiO2) of 35% to have an oxygen saturation (SpO2) of 90-92%.
Intervention Type
Drug
Intervention Name(s)
Poractant Alfa 80 mg/mL Intratracheal Suspension
Intervention Description
Exogenous surfactant (Poractant Alfa) administration at a dose of 200 mg/kg.
Primary Outcome Measure Information:
Title
Respiratory pulmonary function
Description
The oxygen saturation (SpO2) to fraction of inspired oxygen (FiO2) ratio (SFR)
Time Frame
At day 3 of life
Secondary Outcome Measure Information:
Title
Endotracheal intubation
Description
The need of endotracheal intubation after surfactant administration
Time Frame
At day 3, 7 and 28 of life, and at 36 weeks of postmenstrual age or at the discharge if it occurs first
Title
Oxygen therapy
Description
The need of oxygen therapy
Time Frame
At day 3, 7 and 28 of life, and at 36 weeks of postmenstrual age or at the discharge if it occurs first
Title
Respiratory Support-1
Description
The need of respiratory support
Time Frame
At day 3, 7 and 28 of life, and at 36 weeks of postmenstrual age or at the discharge if it occurs first
Title
Respiratory Support-1
Description
Oxygenation index as indicator of the intensity of ventilatory
Time Frame
At day 3, 7 and 28 of life, and at 36 weeks of postmenstrual age or at the discharge if it occurs first
Title
Respiratory severity-1
Description
Silvermann score as secondary respiratory severity index
Time Frame
At day 3, 7 and 28 of life, and at 36 weeks of postmenstrual age or at the discharge if it occurs first
Title
Respiratory severity-2
Description
Lung ultrasound score (LUS) score as secondary respiratory severity index
Time Frame
At day 3, 7 and 28 of life, and at 36 weeks of postmenstrual age or at the discharge if it occurs first
Title
Long-term respiratory pulmonary function
Description
The oxygen saturation (SpO2) to fraction of inspired oxygen (FiO2) ratio (SFR)
Time Frame
At day 7 and 28 of life, and at 36 weeks of postmenstrual age or at the discharge if it occurs first, and 1 year of corrected age
Title
Complications of prematurity
Description
The incidence of intraventricular hemorrhage of grade 3-4, periventricular leukomalacia, bronchopulmonary dysplasia, sepsis and retinopathy of prematurity
Time Frame
From birth to 36 weeks of postmenstrual age or discharge if it occurred first
Title
In-hospital death
Description
death before 36 weeks of gestation
Time Frame
From birth to 36 week of gestation or discharge if it occurred first
10. Eligibility
Sex
All
Minimum Age & Unit of Time
24 Weeks
Maximum Age & Unit of Time
32 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
gestational age less than 32 weeks;
diagnosis of respiratory distress (RDS);
need for ventilatory support;
written informed consent.
Exclusion Criteria:
congenital malformations;
genetic disorders;
perinatal asphyxia.
neonatal pneumonia or wet lung or meconium aspiration syndrome at birth.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Virgilio Carnielli, MD, PHD
Phone
0715962045
Email
v.carnielli@staff.univpm.it
First Name & Middle Initial & Last Name or Official Title & Degree
Valentina Dell'Orto, MD
Phone
0715962014
Email
valentinagiovanna.dellorto@ospedaliriuniti.marche.it
12. IPD Sharing Statement
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Medium vs Low Oxygen Threshold for the Surfactant Administration
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