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Clinical Trials/NCT04315636
NCT04315636
Completed
Phase 3

Surfactant Nebulization for the Early Aeration of the Preterm Lung: a Single Blinded, Parallel, Randomized Controlled Trial

University of Zurich1 site in 1 country32 target enrollmentMarch 19, 2021

Overview

Phase
Phase 3
Intervention
Surfactant nebulisation
Conditions
Preterm Birth
Sponsor
University of Zurich
Enrollment
32
Locations
1
Primary Endpoint
EIT: End-expiratory lung impedance (EELI)
Status
Completed
Last Updated
last year

Overview

Brief Summary

Respiratory distress syndrome is the most common cause of respiratory failure in preterm infants. Treatment consists of respiratory support and exogenous surfactant administration. Commonly, surfactant is administered via an endotracheal tube during mechanical ventilation. However, mechanical ventilation is considered an important risk factor for developing bronchopulmonary dysplasia.

Surfactant nebulisation during noninvasive ventilation may offer an alternative method for surfactant administration and has been shown to be promising in terms of physiological as well as clinical changes. In preterm infants with respiratory distress syndrome, the effect of intratracheally administered surfactant on lung function during invasive ventilation has been studied extensively. However, the effect of early postnatal surfactant nebulization remains unclear.

Therefore, the investigators plan to conduct a randomized controlled trial in order to investigate the effect of surfactant nebulization immediately after birth on early postnatal lung volume and short-term respiratory stability.

Registry
clinicaltrials.gov
Start Date
March 19, 2021
End Date
January 16, 2022
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • gestational age at birth from 26 0/7 to 31 6/7 weeks
  • written informed consent

Exclusion Criteria

  • severe congenital malformation adversely affecting surfactant nebulisation or life expectancy
  • a priori palliative care
  • genetically defined syndrome

Arms & Interventions

Surfactant nebulisation

The experimental group will receive a positive end-expiratory pressure (PEEP, +/- noninvasive positive pressure ventilation) and nebulised surfactant via a customised vibrating membrane nebuliser. Nebulisation will commence with the first application of a PEEP and will continue for a maximum of 30 minutes.

Intervention: Surfactant nebulisation

Outcomes

Primary Outcomes

EIT: End-expiratory lung impedance (EELI)

Time Frame: Between birth and 30 minutes of life.

Change in EELI using electrical impedance tomography (arbitrary units per kilogram)

Secondary Outcomes

  • EIT: End-expiratory lung impedance (EELI)(At 6, 12, and 24 hours of life and at 36 weeks postmenstrual age)
  • Clinical: Number of episodes of desaturation and bradycardia(During the first 24 hours of life.)
  • Clinical: Bronchopulmonary dysplasia (BPD)(At 36 weeks postmenstrual age.)
  • Clinical: Intraventricular haemorrhage (IVH)(At 36 weeks postmenstrual age.)
  • Clinical: Retinopathy of prematurity (ROP)(At 36 weeks postmenstrual age.)
  • Clinical: Necrotizing enterocolitis (NEC)(At 36 weeks postmenstrual age.)
  • EIT: Regional ventilation distribution(At 6, 12, and 24 hours of life and at 36 weeks postmenstrual age.)
  • EIT: Tidal volumes(At 6, 12, and 24 hours of life and at 36 weeks postmenstrual age.)
  • EIT: Association between EELI losses and SpO2/FiO2 ratio.(At 6, 12, and 24 hours of life.)
  • EIT: Association between EELI losses and need/level of respiratory support.(At 6, 12, and 24 hours of life.)
  • Physiological: Oxygen saturation (SpO2)(For the first 30 minutes after birth, and at 6, 12, and 24 hours of life.)
  • Physiological: Fraction of inspired oxygen(For the first 30 minutes after birth, and at 6, 12, and 24 hours of life.)
  • Respiratory: PIP (peak inspiratory pressure)(At 6, 12, and 24 hours of life.)
  • Respiratory: Respiratory rate(At 6, 12, and 24 hours of life.)
  • Clinical: Length and type of noninvasive respiratory support(During the first 30 minutes of life.)
  • Clinical: Total time on noninvasive and invasive respiratory support(Until 36 weeks postmenstrual age)
  • Clinical: Frequency and duration of facemask repositioning(During the first 30 minutes after birth.)
  • Clinical: Intubation(At 24 and 72 hours of life, at 7 days of life. Until 36 weeks postmenstrual age.)
  • Clinical: Time to first intubation(From birth until 36 weeks postmenstrual age.)
  • Clinical: Blood-culture positive sepsis(At 36 weeks postmenstrual age.)
  • Physiological: Heart rate(For the first 30 minutes after birth, as well as at 6, 12, and 24 hours of life.)
  • Physiological: SpO2/FiO2 ratio(At 6, 12, and 24 hours of life.)
  • Respiratory: Positive end-expiratory pressure (PEEP)(During the first 30 minutes of life.)
  • Respiratory: Tidal volume (Vt)(During the first 30 minutes of life.)
  • Respiratory: PEEP (positive end-expiratory pressure)(At 6, 12, and 24 hours of life.)
  • Physiological: Body temperature(In the delivery room.)
  • Respiratory: Peak inspiratory pressure (PIP)(During the first 30 minutes of life.)

Study Sites (1)

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