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Infant Pulmonary Mechanics: High Flow Nasal Cannula Versus Nasal CPAP

Primary Purpose

Respiratory Distress, Lung Injury

Status
Withdrawn
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Heated Humidified High Flow Nasal Cannula
Nasal Continuous Positive Airway Pressure
Sponsored by
Children's Hospital of Philadelphia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Respiratory Distress focused on measuring respiratory distress, Heated Humidified High Flow Nasal Cannula (HHHFNC), HHHFNC, noninvasive nasal continuous positive airway pressure (NCPAP), NCPAP

Eligibility Criteria

2 Hours - 72 Hours (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Birth weight greater than or equal to 1000 grams.
  2. Gestational age at birth between 28 weeks and 37 weeks (28 0/7 to 37 6/7 weeks inclusive).
  3. Candidate for non-invasive respiratory support as a result of:

    1. An intention to manage the infant with non-invasive (no endotracheal tube) respiratory support.
    2. An intention to extubate an infant being managed with intubated respiratory support to non-invasive respiratory support.
  4. Subjects must have a guardian or acceptable surrogate capable of giving consent on his/her behalf.

Exclusion Criteria:

  1. Birth weight less than 1000 grams.
  2. Estimated gestation at birth less than 28 weeks or greater than 37 6/7 weeks.
  3. Active air leak syndrome.
  4. Subjects will not be eligible if they are not considered viable.
  5. Infants with abnormalities of the upper and lower airways
  6. Infants with significant abdominal or respiratory malformations .

Sites / Locations

  • Pennsylvania Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

HHHFNC

NCPAP

Arm Description

Treatment of respiratory distress by Heated Humidified High Flow Nasal Cannula (HHHFNC). Escalation of the ventilatory support per protocol and the attending physician.

Treatment of respiratory distress by nasal continuous positive airway pressure (NCPAP). Escalation of the ventilatory support per protocol and the attending physician.

Outcomes

Primary Outcome Measures

Pulmonary mechanics and chest wall asynchrony measures.
Pulmonary mechanics measures consisting of dynamic lung compliance, airway resistance, and work of breathing and chest wall asynchrony measures consisting of thoracoabdominal asynchrony, labored breathing index and rib cage to abdominal phase relation during the total breath are measured in preterm infants treated with HHHFNC and compared to the same measurements in preterm infants treated with NCPAP.

Secondary Outcome Measures

Duration of respiratory support or oxygen use up to the time of discharge from the NICU.
The total number of days while infants are on any type of respiratory support or oxygen use prior to discharge in preterm infants treated with HHHFNC compared to NCPAP during their hospital stay.
The incidence of potential adverse outcomes associated with HHHFNC or NCPAP.
The number and percentage of infants in each group with adverse effects such as facial and upper airways injury associated with the use of HHHFNC or NCPAP.
Time needed to establish full enteral feeds
The total number of days needed to establish full enteral feeds in preterm infants treated with HHHFNC as compared to preterm infants treated with NCPAP.

Full Information

First Posted
August 30, 2013
Last Updated
September 14, 2015
Sponsor
Children's Hospital of Philadelphia
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1. Study Identification

Unique Protocol Identification Number
NCT01939067
Brief Title
Infant Pulmonary Mechanics: High Flow Nasal Cannula Versus Nasal CPAP
Official Title
Pulmonary Mechanics in Preterm Infants Treated With Heated Humidified High Flow Nasal Cannula as Compared to Nasal Continuous Positive Airway Pressure.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2015
Overall Recruitment Status
Withdrawn
Why Stopped
Application for regulatory approval withdrawn
Study Start Date
March 2014 (undefined)
Primary Completion Date
March 2014 (Actual)
Study Completion Date
March 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital of Philadelphia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is designed to evaluate the effect of heated humidified high flow nasal cannula (HHHFNC) as compared to noninvasive nasal continuous positive airway pressure (NCPAP) on lung function as a measure of lung injury in preterm infants born at 28 to 37 weeks gestation requiring continuing respiratory support.
Detailed Description
Respiratory distress and the need for respiratory support continues to be a common problem for preterm infants. Presence of the breathing tube and duration of respirator provided breaths have been shown to be associated with increased risk for secondary lung injury and subsequent development of chronic lung disease of prematurity. Early application of noninvasive nasal continuous positive airway pressure (NCPAP) has been shown to be an effective, non-invasive, mode of respiratory support in preterm infants and to be associated with a lower incidence of chronic lung disease. A recently published large randomized multicenter study concluded that, among infants born at 28 weeks and longer gestation, heated humidified high flow nasal cannula (HHHFNC) had similar clinical efficacy and safety as compared to NCPAP. Both NCPAP and HHHFNC are currently used to assist infants with breathing problems. This study is designed to evaluate the effect of HHHFNC as compared to NCPAP on lung function as a measure of lung injury in preterm infants born at 28 to 37 weeks gestation requiring continuing respiratory support. In this study, infants will remain on the assigned treatment of either NCPAP or HHHFNC until they require more support as provided by a respirator or until a treatment cross-over from NCPAP to HHHFNC, or the reverse, as decided by their attending physician. The infant's respiratory support will be managed according to his/her attending doctor as per accepted standards of care. A pulmonary function test will be performed twice weekly on each enrolled infant while receiving either NCPAP or HHHFNC support, followed-up by once weekly lung function measurements post respiratory support while infants are breathing only room air until discharge.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Distress, Lung Injury
Keywords
respiratory distress, Heated Humidified High Flow Nasal Cannula (HHHFNC), HHHFNC, noninvasive nasal continuous positive airway pressure (NCPAP), NCPAP

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
HHHFNC
Arm Type
Other
Arm Description
Treatment of respiratory distress by Heated Humidified High Flow Nasal Cannula (HHHFNC). Escalation of the ventilatory support per protocol and the attending physician.
Arm Title
NCPAP
Arm Type
Other
Arm Description
Treatment of respiratory distress by nasal continuous positive airway pressure (NCPAP). Escalation of the ventilatory support per protocol and the attending physician.
Intervention Type
Device
Intervention Name(s)
Heated Humidified High Flow Nasal Cannula
Intervention Description
Biweekly measurement of lung mechanics (dynamic compliance, airway resistance, work of breathing) and chest wall asynchrony measures while on HHHFNC and weekly when weaned off until 40 weeks post conceptional age or discharge. Recording of the level and the type of respiratory support and all cross over respiratory support devices. Recording of all growth parameters, neonatal morbidities and therapies.
Intervention Type
Device
Intervention Name(s)
Nasal Continuous Positive Airway Pressure
Intervention Description
Biweekly measurement of lung mechanics (dynamic compliance, airway resistance, work of breathing) and chest wall asynchrony measures while on NCPAP and weekly when weaned off until 40 weeks post conceptional age or discharge. Recording of the level and the type of respiratory support and all cross over respiratory support devices. Recording of all growth parameters, neonatal morbidities and therapies.
Primary Outcome Measure Information:
Title
Pulmonary mechanics and chest wall asynchrony measures.
Description
Pulmonary mechanics measures consisting of dynamic lung compliance, airway resistance, and work of breathing and chest wall asynchrony measures consisting of thoracoabdominal asynchrony, labored breathing index and rib cage to abdominal phase relation during the total breath are measured in preterm infants treated with HHHFNC and compared to the same measurements in preterm infants treated with NCPAP.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Duration of respiratory support or oxygen use up to the time of discharge from the NICU.
Description
The total number of days while infants are on any type of respiratory support or oxygen use prior to discharge in preterm infants treated with HHHFNC compared to NCPAP during their hospital stay.
Time Frame
2 years
Title
The incidence of potential adverse outcomes associated with HHHFNC or NCPAP.
Description
The number and percentage of infants in each group with adverse effects such as facial and upper airways injury associated with the use of HHHFNC or NCPAP.
Time Frame
2 years
Title
Time needed to establish full enteral feeds
Description
The total number of days needed to establish full enteral feeds in preterm infants treated with HHHFNC as compared to preterm infants treated with NCPAP.
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Hours
Maximum Age & Unit of Time
72 Hours
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Birth weight greater than or equal to 1000 grams. Gestational age at birth between 28 weeks and 37 weeks (28 0/7 to 37 6/7 weeks inclusive). Candidate for non-invasive respiratory support as a result of: An intention to manage the infant with non-invasive (no endotracheal tube) respiratory support. An intention to extubate an infant being managed with intubated respiratory support to non-invasive respiratory support. Subjects must have a guardian or acceptable surrogate capable of giving consent on his/her behalf. Exclusion Criteria: Birth weight less than 1000 grams. Estimated gestation at birth less than 28 weeks or greater than 37 6/7 weeks. Active air leak syndrome. Subjects will not be eligible if they are not considered viable. Infants with abnormalities of the upper and lower airways Infants with significant abdominal or respiratory malformations .
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Soraya Abbasi, MD
Organizational Affiliation
University of Pennsylvania
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pennsylvania Hospital
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19107
Country
United States

12. IPD Sharing Statement

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Infant Pulmonary Mechanics: High Flow Nasal Cannula Versus Nasal CPAP

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