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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
Virgilio Paolo Carnielli
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Respiratory Distress Syndrome focused on measuring RDS, Surfactant, Threshold, Oxygen, Preterm, Infant

Eligibility Criteria

24 Weeks - 32 Weeks (Child)All SexesDoes not accept healthy volunteers

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

    First Posted
    December 12, 2019
    Last Updated
    April 15, 2021
    Sponsor
    Virgilio Paolo Carnielli
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    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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