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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03242057
Other study ID # IRB201701971
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 23, 2017
Est. completion date September 5, 2019

Study information

Verified date February 2020
Source University of Florida
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Extubation failure is a significant problem in preterm neonates and prolonged intubation is a well-documented risk factor for development of chronic lung disease. Out of the respiratory modalities available to extubate a preterm neonate; high flow nasal canula, nasal continuous positive airway pressure (nCPAP) and noninvasive positive pressure ventilation (NIPPV) are the most commonly used.

A recent Cochrane meta-analysis concluded that NIPPV has lower extubation failure as compared to nCPAP (30% vs. 40%)

NAVA (neurally adjusted ventilatory assist), a relatively new mode of mechanical ventilation in which the diaphragmatic electrical activity initiates a ventilator breath and adjustment of a preset gain (NAVA level) determines the peak inspiratory pressure. It has been reported to improve patient - ventilator synchrony and minimize mean airway pressure and ability to wean an infant from a ventilator. However till date there has been no head to head comparison of extubation failure in infants managed on NAVA with conventional ventilator strategies.

In this study the investigators aim to compare primary extubation failure rates in infants/participants managed by NIPPV vs. NI-NAVA (non invasive NAVA). Eligible infants/participants will be randomized to be extubated to predefined NIPPV or NI-NAVA ventilator settings and will be assessed for primary extubation failure (defined as reintubation within 5 days after an elective extubation).


Description:

Mechanical ventilation is needed for most preterm infants to maintain adequate oxygenation and ventilation. However the coexistence of lung immaturity, weak respiratory drive, excessively compliant chest wall, and surfactant deficiency often contribute to dependency on mechanical ventilation during the first days or weeks after birth.

Prolonged mechanical ventilation is associated with high mortality and morbidities including ventilator-associated pneumonia, pneumothorax, and bronchopulmonary dysplasia (BPD). Each additional week of mechanical ventilation is reported to be associated with an increase in the risk of neurodevelopmental impairment. Reduction in the need and duration of invasive mechanical ventilation may potentially improve outcome of preterm infants.

Extubation failure has been independently associated with increased mortality, longer hospitalization, and more days on oxygen and ventilatory support. It is critical, therefore, to attempt extubation early and at a time when successful extubation is likely.

A recent Cochrane review compared the use of nasal intermittent positive pressure ventilation (NIPPV) with nasal continuous positive airway pressure (nCPAP) in preterm infants after extubation and found that NIPPV may be more effective than nCPAP at decreasing extubation failure.

The feasibility of NAVA use has been described in neonatal and pediatric patients. Several studies cite a decrease in peak inspiratory pressures, improved synchrony in triggering, and more appropriate termination of positive pressure support. Some studies have reported lower work of breathing, PaO2/FiO2 ratios (partial pressure of oxygen/ fractional inspired oxygen)and MAP. In addition, NAVA has been used for patients who "fight the ventilator," and the synchrony improves the ability to wean.

The use of NIV-NAVA in neonates has promise as a primary mode of ventilation to aid in the prevention of intubation and also maintaining successful extubation. Early extubation may be enhanced with NIV-NAVA of those neonates requiring intubation for numerous reasons. The ability to provide synchronous NIV allows clinicians the opportunity to extubate infants earlier with increased confidence than with previous post extubation support.

However there is lack of scientific evidence on extubation failure rates on NI-NAVA. Trials comparing NAVA to conventional ventilators with regard to ventilator associated lung injury, ventilator associated pneumonia and decreasing duration of time on the ventilator have not yet been reported.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date September 5, 2019
Est. primary completion date September 5, 2019
Accepts healthy volunteers No
Gender All
Age group 24 Weeks to 32 Weeks
Eligibility Inclusion Criteria:

1. Infants born between 24 weeks and = 32 weeks completed gestational age or birth weight less than or equal to 1500 grams

2. Postnatal age = 14 days

3. Inborn

4. Mechanically ventilated for at least 12 hrs.

5. Intubated within first 24 hrs. after birth

6. Outborn infants intubated and transferred to UF within 24 hrs. after birth.

Exclusion Criteria:

1. Outborn > 24hrs of age.

2. Failed elective extubation prior to study enrollment

3. Major congenital anomalies or known/suspected chromosomal anomalies

4. Use of paralytics in previous 24 hrs.

5. Participation in another randomized interventional trial

6. Known or suspected phrenic nerve palsy or lesion

7. Known or suspected diaphragmatic lesion

8. Any contraindication to have a nasogastric or orogastric tube placement

Study Design


Intervention

Other:
NAVA
Infant will be extubated to NAVA, settings based per protocol
NIPPV
Infant will be extubated to NIPPV, settings detailed in protocol

Locations

Country Name City State
United States University of Florida Jacksonville Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Florida

Country where clinical trial is conducted

United States, 

References & Publications (9)

Baudin F, Pouyau R, Cour-Andlauer F, Berthiller J, Robert D, Javouhey E. Neurally adjusted ventilator assist (NAVA) reduces asynchrony during non-invasive ventilation for severe bronchiolitis. Pediatr Pulmonol. 2015 Dec;50(12):1320-7. doi: 10.1002/ppul.23139. Epub 2014 Dec 8. — View Citation

Bhandari V. Nasal intermittent positive pressure ventilation in the newborn: review of literature and evidence-based guidelines. J Perinatol. 2010 Aug;30(8):505-12. doi: 10.1038/jp.2009.165. Epub 2009 Oct 22. Review. Erratum in: J Perinatol. 2010 Dec;30(12):827. — View Citation

Firestone KS, Beck J, Stein H. Neurally Adjusted Ventilatory Assist for Noninvasive Support in Neonates. Clin Perinatol. 2016 Dec;43(4):707-724. doi: 10.1016/j.clp.2016.07.007. Review. — View Citation

Firestone KS, Fisher S, Reddy S, White DB, Stein HM. Effect of changing NAVA levels on peak inspiratory pressures and electrical activity of the diaphragm in premature neonates. J Perinatol. 2015 Aug;35(8):612-6. doi: 10.1038/jp.2015.14. Epub 2015 Mar 12. — View Citation

Lee J, Kim HS, Jung YH, Shin SH, Choi CW, Kim EK, Kim BI, Choi JH. Non-invasive neurally adjusted ventilatory assist in preterm infants: a randomised phase II crossover trial. Arch Dis Child Fetal Neonatal Ed. 2015 Nov;100(6):F507-13. doi: 10.1136/archdischild-2014-308057. Epub 2015 Jul 15. — View Citation

Lemyre B, Davis PG, De Paoli AG, Kirpalani H. Nasal intermittent positive pressure ventilation (NIPPV) versus nasal continuous positive airway pressure (NCPAP) for preterm neonates after extubation. Cochrane Database Syst Rev. 2017 Feb 1;2:CD003212. doi: 10.1002/14651858.CD003212.pub3. Review. — View Citation

LoVerde B, Firestone KS, Stein HM. Comparing changing neurally adjusted ventilatory assist (NAVA) levels in intubated and recently extubated neonates. J Perinatol. 2016 Dec;36(12):1097-1100. doi: 10.1038/jp.2016.152. Epub 2016 Sep 15. — View Citation

Stein H, Firestone K, Rimensberger PC. Synchronized mechanical ventilation using electrical activity of the diaphragm in neonates. Clin Perinatol. 2012 Sep;39(3):525-42. doi: 10.1016/j.clp.2012.06.004. Review. — View Citation

Stein H, Firestone K. Application of neurally adjusted ventilatory assist in neonates. Semin Fetal Neonatal Med. 2014 Feb;19(1):60-9. doi: 10.1016/j.siny.2013.09.005. Epub 2013 Nov 13. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Extubation success assess how many infants stayed extubated at 5 days after extubation 5 days
Secondary Bronchopulmonary dysplasia (BPD) based on NIH guidelines until discharge / 36 weeks post menstrual age
Secondary Ventilator Days days on positive pressure ventilation until discharge / 36 weeks post menstrual age
Secondary NICU length of stay discharge or death or transfer until discharge / 36 weeks post menstrual age
Secondary Patent ductus arteriosus (PDA) echo diagnosed/confirmed until discharge / 36 weeks post menstrual age
Secondary Necrotizing enterocolitis (NEC confirmed on Xray until discharge / 36 weeks post menstrual age
Secondary Late onset sepsis only culture proven until discharge / 36 weeks post menstrual age
Secondary Gastrointestinal perforation confirmed on X-ray or surgical exploration until discharge / 36 weeks post menstrual age
Secondary Mortality all causes within NICU stay until discharge / 36 weeks post menstrual age
Secondary Extubation failure at 3 days reintubation by 72 hrs. post extubation until discharge / 36 weeks post menstrual age
Secondary Extubation failure at 7 days reintubation by 72 hrs. post extubation until discharge / 36 weeks post menstrual age
Secondary Pulmonary air leak including pulmonary interstitial emphysema (PIE) pneumomediastinum and pneumothorax until discharge / 36 weeks post menstrual age
Secondary Severe intraventricular hemorrhage on cranial ultrasound, worst grade until discharge / 36 weeks post menstrual age
Secondary Abdominal distension > 2cm from baseline and with signs necessitating cessation of feeds during the first 48 hrs. after extubation during the first 48 hrs. after extubation until discharge / 36 weeks post menstrual age
Secondary Retinopathy of prematurity (ROP) ophthalmologic exam until discharge / 36 weeks post menstrual age
Secondary Ventilator associated Pneumonia (VAP) diagnosed based on tracheal culture + CXR changes + clinical worsening + treatment until discharge / 36 weeks post menstrual age
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