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High Flow Nasal Cannula Versus Nasal Continuous Positive Airway Pressure for Respiratory Support of Preterm Neonates

A

Ain Shams University

Status

Completed

Conditions

Respiratory Distress Syndrome, Newborn

Treatments

Diagnostic Test: Functional Echocardiography

Study type

Observational

Funder types

Other

Identifiers

NCT04238273
FMASU MD 386/2017

Details and patient eligibility

About

This work is designed to:

  1. Evaluate the efficacy of HHHFNC in comparison with nCPAP in preterm neonates.
  2. Investigate hemodynamic changes associated with HHHFNC in comparison to nCPAP in preterm neonates during periods of non-invasive respiratory support and after being off support.

Full description

There is a preference of using noninvasive modes of ventilation for management of respiratory distress syndrome (RDS) in preterm infants and of weaning of ventilated neonates as soon as possible to non-invasive modes.

Yet, little is known about which non-invasive mode is better and the hemodynamic changes that occur to the infants secondary to these modes. The study provides an evaluation of the efficacy of heated, humidified high flow nasal cannula (HHHFNC) in comparison to nasal continuous positive airway pressure (nCPAP) in preterm infants. Secondary aim is to assess echographic, cerebral blood flow and mesenteric blood flow changes during HHHFNC versus nCPAP.

Enrollment

123 patients

Sex

All

Ages

Under 4 weeks old

Volunteers

No Healthy Volunteers

Inclusion criteria

Infants are eligible if they meet the following criteria:

  1. Gestational age ≤ 35 weeks.
  2. Preterm neonates in need for non invasive ventilation whether they were on invasive ventilatory support before or not.

Exclusion criteria

Preterm neonates with evidence of any of the following will be excluded:

  1. Major upper or lower airway anomalies.
  2. Significant congenital anomalies including cardiac, abdominal or respiratory.
  3. Hemodynamically significant patent ductus arteriosus (PDA): diagnosed if there is colour doppler echocardiographic evidence of left to right ductal shunt, ductal diameter >1.5mm/kg or left atrial/aortic root ratio >1.4

Trial design

123 participants in 2 patient groups

HHHFNC
Description:
it included 63 preterm neonates on Heated, Humidified High Flow Nasal Cannula, of which 35 preterm underwent functional echocardiography, transcranial ultrasonography Doppler applied to the anterior cerebral artery and assessment of pre-prandial superior mesenteric artery velocity and volume of blood flow with Doppler sonography. All of which done while on non invasive ventilation and after weaning.
Treatment:
Diagnostic Test: Functional Echocardiography
NCPAP
Description:
it included 60 preterm neonates on Nasal Continuous Positive Airway Pressure, of which 35 preterm underwent functional echocardiography, transcranial ultrasonography Doppler applied to the anterior cerebral artery and assessment of pre-prandial superior mesenteric artery velocity and volume of blood flow with Doppler sonography. All of which done while on non invasive ventilation and after weaning.
Treatment:
Diagnostic Test: Functional Echocardiography

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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