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Inhaled Steroids for the Treatment of Early Pediatric Acute Respiratory Distress Syndrome

Primary Purpose

Acute Respiratory Distress Syndrome

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Budesonide
Placebo
Nebulizer
Sponsored by
The University of Texas Health Science Center, Houston
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Respiratory Distress Syndrome focused on measuring Pediatric acute respiratory distress syndrome, PARDS, Budesonide, inhaled steroids

Eligibility Criteria

30 Days - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Pediatric patients older than 30 days and up to 18 years of age admitted to the PICU with a diagnosis of PARDS enrolled within 72 hours of diagnosis.
  • Patients requiring invasive mechanical ventilation.
  • Criteria of PARDS as defined by the Pediatric Acute Lung Injury Consensus Conference (PALICC), on June 2015 in Pediatric Critical Care Journal

Exclusion Criteria:

  • Patients with diffuse alveolar hemorrhage.
  • Patients terminally ill with limitation of care or in hospice care.
  • Patients receiving inhaled steroids or systemic steroids as chronic therapy before admission.
  • Patients with high dose systemic steroids for anti-inflammatory purposes. The investigators will not exclude patients receiving hydrocortisone for shock.

Sites / Locations

  • The University of Texas Health Science Center at Houston

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Budesonide administered by nebulizer

Placebo administered by nebulizer

Arm Description

Outcomes

Primary Outcome Measures

Number of Ventilator-free Days (VFD)

Secondary Outcome Measures

Oxygenation Index (OI)
Oxygenation index (OI) is calculated as ([FiO2 x Mean Airway Pressure] / PaO2). FiO2 stands for inspired fraction of oxygen, and PaO2 stands for pressure/arterial pressure of oxygen. An oxygenation index of 4-8 indicates mild ARDS, an oxygenation index of 8-16 indicates moderate ARDS, and an oxygenation index greater than 16 indicates severe ARDS.
Oxygen Saturation Index (OSI)
5-7.5 mild ARDS, 7.5-12.3 moderate ARDS. > 12.3 severe ARDS, formula FiO2*Mean airway pressure/Saturation of O2 Oxygen saturation index (OI) is calculated as ([FiO2 x Mean Airway Pressure] / Saturation of oxygen). FiO2 stands for inspired fraction of oxygen. An oxygen saturation index of 5-7.5 indicates mild ARDS, an oxygen saturation index of 7.5-12.3 indicates moderate ARDS, and an oxygen saturation index greater than 12.3 indicates severe ARDS.
Number of Days Participant Stayed in Pediatric Intensive Care Unit (PICU)
Number of Days Participant Stayed in Hospital
TNF Alpha Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
TNF Alpha Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
TNF Alpha Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Interleukin (IL) -6 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
IL-6 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
IL-6 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
IL-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
IL-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
IL-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
MMP-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
MMP-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
MMP-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
MMP-9 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
MMP-9 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
MMP-9 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Neutrophil Count
Neutrophil Count
Neutrophil Count
FEV1
Forced expiration in 1st second, abnormal (obstructive)<80% L/second
Forced Expiratory Volume at One Second FEV1/FVC
Restrictive disease if <70%
Forced Vital Capacity (FVC)
<80% restrictive lung disease, L
Forced Expiratory Flow FEF 25-75%
Medium size bronchioles, normal 60-130%
Respiratory Resistance by Impulse Oscillometry (IOS)
Rrs 3-35 Hz
Respiratory Impedance by Impulse Oscillometry (IOS)
Zrs 3-35 Hz
Respiratory Reactance by Impulse Oscillometry (IOS)
Xrs 3-35 Hz

Full Information

First Posted
August 16, 2019
Last Updated
June 24, 2022
Sponsor
The University of Texas Health Science Center, Houston
Collaborators
National Center for Advancing Translational Sciences (NCATS)
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1. Study Identification

Unique Protocol Identification Number
NCT04064684
Brief Title
Inhaled Steroids for the Treatment of Early Pediatric Acute Respiratory Distress Syndrome
Official Title
Inhaled Steroids for the Treatment of Early Pediatric Acute Respiratory Distress Syndrome (PARDS), a Randomized Pilot Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Terminated
Why Stopped
Enrollment difficulties after the start of the COVID-19 pandemic.
Study Start Date
February 4, 2020 (Actual)
Primary Completion Date
March 30, 2020 (Actual)
Study Completion Date
March 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Texas Health Science Center, Houston
Collaborators
National Center for Advancing Translational Sciences (NCATS)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No

5. Study Description

Brief Summary
The purpose of this study is to show that inhaled steroids in patient with PARDS can decrease the days on mechanical ventilator measured by ventilator-free days,to improve the oxygenation index (OI) or oxygenation saturation index (OSI) in patients receiving inhaled steroids and to show the relevance and feasibility of a larger study by assessing the hypothesis in a small cohort of patients. Patient will be treated for a maximum of 10 days. Secondary objectives are to reduce the length of stay (LOS) in the pediatric intensive care unit (PICU) and hospital admissions; to show less inflammation in the patients receiving inhaled steroids by measuring inflammatory markers from tracheal aspirates like Interleukin (IL6, IL8, tumor necrosis factor (TNF) α, matrix metalloproteinase8 (MMP8) and matrix metalloproteinase9 (MMP9). Lastly, to show that inhaled steroids can improve residual lung disease evaluated by Pulmonary Function Test (PFTs) and Impulse Oscillometry (IOS).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Distress Syndrome
Keywords
Pediatric acute respiratory distress syndrome, PARDS, Budesonide, inhaled steroids

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Budesonide administered by nebulizer
Arm Type
Experimental
Arm Title
Placebo administered by nebulizer
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Budesonide
Other Intervention Name(s)
Pulmicort Respules®
Intervention Description
Enrolled patients will be treated with Pulmicort Respules® (Budesonide inhalation suspension), at a dose of 0.5 mg, nebulized twice daily through the mechanical ventilator. The medication will be administered to the patient by the respiratory therapist with the single-patient-use medication nebulizer attached to the mechanical ventilator circuit. The maximum length of treatment will be 10 days.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Enrolled patients will be treated with normal saline.The medication will be administered to the patient by the respiratory therapist with the single-patient-use medication nebulizer attached to the mechanical ventilator circuit. The maximum length of treatment will be 10 days.
Intervention Type
Device
Intervention Name(s)
Nebulizer
Intervention Description
The medication will be administered to the patient by the respiratory therapist with the single-patient-use medication nebulizer attached to the mechanical ventilator circuit.
Primary Outcome Measure Information:
Title
Number of Ventilator-free Days (VFD)
Time Frame
Between the time of enrollment and day 28 after enrollment
Secondary Outcome Measure Information:
Title
Oxygenation Index (OI)
Description
Oxygenation index (OI) is calculated as ([FiO2 x Mean Airway Pressure] / PaO2). FiO2 stands for inspired fraction of oxygen, and PaO2 stands for pressure/arterial pressure of oxygen. An oxygenation index of 4-8 indicates mild ARDS, an oxygenation index of 8-16 indicates moderate ARDS, and an oxygenation index greater than 16 indicates severe ARDS.
Time Frame
Day one to last day of last day of mechanical ventilation (up to 10 days)
Title
Oxygen Saturation Index (OSI)
Description
5-7.5 mild ARDS, 7.5-12.3 moderate ARDS. > 12.3 severe ARDS, formula FiO2*Mean airway pressure/Saturation of O2 Oxygen saturation index (OI) is calculated as ([FiO2 x Mean Airway Pressure] / Saturation of oxygen). FiO2 stands for inspired fraction of oxygen. An oxygen saturation index of 5-7.5 indicates mild ARDS, an oxygen saturation index of 7.5-12.3 indicates moderate ARDS, and an oxygen saturation index greater than 12.3 indicates severe ARDS.
Time Frame
Day one to last day of last day of mechanical ventilation up to 28 days since enrollment
Title
Number of Days Participant Stayed in Pediatric Intensive Care Unit (PICU)
Time Frame
from time of enrollment until participant is transferred, discharged, or deceased (up to 50 days)
Title
Number of Days Participant Stayed in Hospital
Time Frame
from time of enrollment until participant is transferred, discharged, or deceased (up to 50 days)
Title
TNF Alpha Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
Day 1
Title
TNF Alpha Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
Day 3
Title
TNF Alpha Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
last day of treatment or last day of invasive mechanical ventilation( upto day 28)
Title
Interleukin (IL) -6 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
Day 1
Title
IL-6 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
Day 3
Title
IL-6 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
last day of treatment or last day of invasive mechanical ventilation( upto day 28)
Title
IL-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
Day 1
Title
IL-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
Day 3
Title
IL-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
last day of treatment or last day of invasive mechanical ventilation( upto day 28)
Title
MMP-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
Day 1
Title
MMP-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
Day 3
Title
MMP-8 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
last day of treatment or last day of invasive mechanical ventilation( upto day 28)
Title
MMP-9 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
Day 1
Title
MMP-9 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
Day 3
Title
MMP-9 Levels as Assessed by the Enzyme-linked Immunosorbent Assay (ELISA) Test
Time Frame
last day of treatment or last day of invasive mechanical ventilation( upto day 28)
Title
Neutrophil Count
Time Frame
Day 1
Title
Neutrophil Count
Time Frame
Day 3
Title
Neutrophil Count
Time Frame
last day of treatment or last day of invasive mechanical ventilation( upto day 28)
Title
FEV1
Description
Forced expiration in 1st second, abnormal (obstructive)<80% L/second
Time Frame
90 days since first day of treatment
Title
Forced Expiratory Volume at One Second FEV1/FVC
Description
Restrictive disease if <70%
Time Frame
90 days since first day of treatment
Title
Forced Vital Capacity (FVC)
Description
<80% restrictive lung disease, L
Time Frame
90 days since first day of treatment
Title
Forced Expiratory Flow FEF 25-75%
Description
Medium size bronchioles, normal 60-130%
Time Frame
90 days since first day of treatment
Title
Respiratory Resistance by Impulse Oscillometry (IOS)
Description
Rrs 3-35 Hz
Time Frame
90 days since first day of treatment
Title
Respiratory Impedance by Impulse Oscillometry (IOS)
Description
Zrs 3-35 Hz
Time Frame
90 days since first day of treatment
Title
Respiratory Reactance by Impulse Oscillometry (IOS)
Description
Xrs 3-35 Hz
Time Frame
90 days since first day of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Days
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pediatric patients older than 30 days and up to 18 years of age admitted to the PICU with a diagnosis of PARDS enrolled within 72 hours of diagnosis. Patients requiring invasive mechanical ventilation. Criteria of PARDS as defined by the Pediatric Acute Lung Injury Consensus Conference (PALICC), on June 2015 in Pediatric Critical Care Journal Exclusion Criteria: Patients with diffuse alveolar hemorrhage. Patients terminally ill with limitation of care or in hospice care. Patients receiving inhaled steroids or systemic steroids as chronic therapy before admission. Patients with high dose systemic steroids for anti-inflammatory purposes. The investigators will not exclude patients receiving hydrocortisone for shock.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alvaro J Coronado Munoz, MD
Organizational Affiliation
The University of Texas Health Science Center, Houston
Official's Role
Principal Investigator
Facility Information:
Facility Name
The University of Texas Health Science Center at Houston
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Inhaled Steroids for the Treatment of Early Pediatric Acute Respiratory Distress Syndrome

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