High Flow Nasal Cannula Versus Nasal Intermittent Positive Pressure (NIPPV) in Preterm Infants (VAPORAM)

Israel Healthcare Foundation

Status: Unknown

Conditions: Preterm Infant

Treatments: Other: Vapotherm; Other: NIPPV

Study type: Interventional

Funder types: Other

Identifiers

NCT03853161

CMC-17-0131-CTIL

Details and patient eligibility

About

The aim of this study is to compare the effectiveness of Heated Humidified High Flow Nasal Cannula (HHHFNC) versus Nasal Intermittent Positive Pressure Ventilation (NIPPV) in preventing intubation when used as primary respiratory support for Respiratory Distress Syndrome (RDS) or post extubation in preterm infants

Full description

Patient population will include preterm infants born at 24 - 36+6 weeks of gestation who are candidates for non-invasive respiratory support post extubation or as primary respiratory support after birth. They will be will be randomized to 2 groups: Heated Humidified High Flow Nasal Cannula (HHHFNC) and Nasal Intermittent Positive Pressure Ventilation (NIPPV).

This will be a prospective unblinded randomized controlled study, designed as a non-inferiority trial.

Primary outcome: The primary outcome will be rate of treatment failure (need for intubation) within 7 days of starting the study treatment

Enrollment: 130 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Infants born at 24-27+6 weeks of gestation and up to 28 days of life who are extubated for the first time after birth or immediately after surfactant administration via (intubation-surfactant-extubation) INSURE or (minimally invasive surfactant therapy) MIST procedures.
• Infants born at 28-36+6 weeks of gestation and up to 28 days of life who are candidates for non-invasive support either as a primary modality after birth or post extubation.
• Signed parental informed consent by one of the parents

Exclusion criteria

• Infants who are unlikely to survive the immediate postnatal period or who have significant congenital abnormalities
• Presence of a pneumothorax prior to enrollment
• Hemodynamic instability due to sepsis or hemorrhage
• Inability to obtain parental consent
• Shortage of suitable equipment
• Infants who were intubated solely for surgery

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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130 participants in 2 patient groups

Vapotherm arm

Experimental group

Description:

Preterm infants in this arm will be given respiratory support of heated humidified high flow via Precision Flow Vapotherm, Exeter, USA

Treatment:

Other: Vapotherm

NIPPV arm

Experimental group

Description:

Preterm infants in this arm will be given respiratory support of Nasal Intermittent Positive Pressure Ventilation via the Leoni Plus neonatal ventilator

Treatment:

Other: NIPPV