Comparison Between Infant Flow SiPAP and Noninvasive NAVA in the Neonatal Intensive Care Unit

NCT01588080 | Completed

• 1 other identifier: NAVA
• Study Type: interventional
• Target: 21
• Locations: 1 country
• Sites: 2

Brief Summary

When babies are born premature, they often need help with their breathing. The equipment used to help them breathe is not very comfortable and they sometimes need to be put on a specialized breathing machine with a tube into their lungs. The breathing machine or ventilator can be damaging to the newborn's lungs and more damage can occur the longer the newborn stays on a ventilator leading to chronic lung disease later in their lives. A new device called neurally adjusted ventilatory assist or NAVA is available that the investigators believe may be more comfortable for the premature newborn and may help the baby come off breathing support sooner. When using this device, babies may not need to be put on a ventilator and can avoid the lung damage associated with the breathing tube and the ventilator. The objective of this pilot study is to compare this new breathing device called NAVA, to the equipment that is currently being used, called SiPAP, to support premature newborn's breathing after birth without a breathing tube. The investigators hope to show that with this new technology, premature newborns that are having a difficult time breathing, will come off breathing support sooner compared to the breathing machines that are currently being used. The hypothesis for this proposed study is that improved synchrony with noninvasive NAVA will decrease time spent on noninvasive ventilation and avoid intubation.

Conditions

Respiratory Distress Syndrome

Outcome Measures

Primary Outcomes (1)

• total duration of respiratory support which includes both days and hours on NAVA/SiPAP (DORS)

  one year

Secondary Outcomes (10)

• Proportion of infants that required escalation to increased noninvasive respiratory support (BiPhasic or increasing NAVA levels) or intubation and mechanical ventilation

  one year

• All cause mortality during the hospitalization

  one year

• Bronchopulmonary dysplasia defined as oxygen requirements or ventilatory support needs at 36 weeks CGA

  one year

• Number of doses of surfactant

  one year

• Incidence of pneumothorax

  one year

Study Arms (2)

SiPAP

PLACEBO COMPARATOR

Device: SiPAP - placebo

Neurally Adjusted Ventilatory Assist

EXPERIMENTAL

Device: Neurally Adjusted Ventilatory Assist (NAVA)

Interventions

Neurally Adjusted Ventilatory Assist (NAVA) DEVICE

Neurally adjusted ventilatory assist (NAVA), an adjunct that can only be used with the Servo-i ventilator, allows the patient to synchronize spontaneous respiratory effort with mechanical ventilation. NAVA uses the electromyographic signal of the diaphragm (Edi) to transmit this electrical activity back to the ventilator. The NAVA catheter is a functional gastric tube that has electrodes embedded within it and positioned at the level of diaphragm using an electrocardiogram signal. These electrodes continuously (every 5ms) detect the amplitude, duration, and frequency of the Edi and provide pressure support in proportion to this electrical activity. Proportionality is controlled by a NAVA factor (cmH20/microvolt) and is adjusted by the user.

Neurally Adjusted Ventilatory Assist

SiPAP - placebo DEVICE

The Infant Flow® SiPAP provides noninvasive support to neonates. CPAP and Biphasic modes are provided by the Infant Flow® SiPAP. CPAP is an elevated pressure (above atmospheric) and is used to increase a premature babies functional residual capacity (FRC). CPAP is a modality used for babies with both central apneas and mild/moderate increase work of breathing. CPAP increases the FRC and ultimately recruits collapsed alveoli and improves gas exchange in the lungs. BiPhasic, on the other hand, is a modality used for babies that require more respiratory support than CPAP can provide. In BiPhasic mode, respiratory rate (RR), inspiratory time (Ti), and peak inspiratory pressures (PIP) are set and not synchronized with the patients breathing efforts.

SiPAP

Eligibility Criteria

• Age: 28 Weeks - 32 Weeks
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17)

You may qualify if:

• Infants born greater than or equal to 28+0 weeks and less than or equal to 31+6 weeks gestation
• Diagnosis of RDS in the first 24 hours of life requiring respiratory support
• Parental consent obtained

You may not qualify if:

• Infants with a major congenital anomaly
• Infants with pulmonary hypoplasia
• Infants known or suspected to have a neuromuscular disorder
• Infants less than 28+0 weeks GA
• Intubated infants that are likely to require continued mechanical ventilation
• Infants requiring vigorous resuscitation at birth, including chest compressions +/- cardiac medications

Sponsors & Collaborators

• Fraser Health: lead

Study Sites (2)

Surrey Memorial Hospital

Surrey, British Columbia, V3V 1Z2, Canada

Location

Surrey Memorial Hospital

Surrey, British Columbia, V3V1Z2, Canada

Location

MeSH Terms

Conditions

Respiratory Distress Syndrome

Interventions

Interactive Ventilatory Support

Condition Hierarchy (Ancestors)

Lung Diseases; Respiratory Tract Diseases; Respiration Disorders

Intervention Hierarchy (Ancestors)

Respiration, Artificial; Airway Management; Therapeutics; Respiratory Therapy

Study Officials

• Ravinder Kajla

  Fraser Health

  PRINCIPAL INVESTIGATOR

• Rebecca Sherlock, MD

  Fraser Health

  STUDY CHAIR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Respiratory Therapist, Clinical Resource Therapist

Study Record Dates

• First Submitted: April 26, 2012
• First Posted: April 30, 2012
• Study Start: July 1, 2012
• Primary Completion: November 1, 2014
• Study Completion: November 1, 2014
• Last Updated: May 27, 2015

Record last verified: 2015-05

Locations

CA (2)