Evidence map›Paper›PMID 36714639›Full record

ArticleFrontiers in pediatrics2022

Protocol for a multicenter, double-blind, randomized, placebo-controlled phase III trial of the inhaled β2-adrenergic receptor agonist salbutamol for transient tachypnea of the newborn (the REFSAL trial).

Dariusz Madajczak, Thierry Daboval, Ryszard Lauterbach, Beata Łoniewska, Witold Błaż, Tomasz Szczapa, Iwona Sadowska-Krawczenko, Marzena Michalak-Kloc, Helena Sławska, Maria Borszewska-Kornacka and 2 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05527704 (a Multicentre, Double-blind, Randomized, Placebo-controlled Phase III Trial of the Inhaled β2-adrenergic Receptor Agonist Salbutamol for Transient Tachypnoea of the Newborn), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.3field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05527704 phase3active not recruitingnot on this map

a Multicentre, Double-blind, Randomized, Placebo-controlled Phase III Trial of the Inhaled β2-adrenergic Receptor Agonist Salbutamol for Transient Tachypnoea of the Newborn (the REFSAL Trial)

TypeinterventionalSponsorMedical University of WarsawRan2021 to 2026Enrolled608ConditionsTTN, Respiratory Failure, PPHNArmsSalbutamol, 0,9% Chloride Sodium
3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 8 institutions in 2 countries.

Dariusz MadajczakDepartment of Neonatology and Neonatal Intensive Care, Medical University of Warsaw, Warsaw, Poland.
Thierry DabovalDepartment of Pediatrics - Division of Neonatology, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Ryszard LauterbachNeonatology Clinic, University Hospital, Krakow, Poland.
Beata ŁoniewskaDepartment of Neonatology and Intensive Neonatal Care, Pomeranian Medical University, Szczecin, Poland.
Witold BłażClinical Department of Neonatology With Neonatal Intensive Care Unit, University of Rzeszow, Saint Jadwiga the Queen Clinical Provincial Hospital No 2, Rzeszow, Poland.
Tomasz SzczapaDepartment of Neonatology, Poznań University of Medical Sciences, Poznań, Poland.
Iwona Sadowska-KrawczenkoDepartment of Neonatology, Collegium Medicum in Bydgoszcz, Nicolaus Copernicus University, Toruń, Poland.
Marzena Michalak-KlocNeonatology Clinical Department, Karol Marcinkowski University Hospital, Zielona Góra, Poland.
Helena SławskaNeonatology Unit, Specialist Hospital No 2, Bytom, Medical University of Silesia, Bytom, Poland.
Maria Borszewska-KornackaDepartment of Neonatology and Neonatal Intensive Care, Medical University of Warsaw, Warsaw, Poland.
Renata BokiniecDepartment of Neonatology and Neonatal Intensive Care, Medical University of Warsaw, Warsaw, Poland.
REFSAL Study Group
Medical University of Warsaw · PLGrochowski Hospital · PLNicolaus Copernicus University · PLPomeranian Medical University · PLPoznan University of Medical Sciences · PLRzeszów University · PLUniversity of Ottawa · CAWojewódzki Szpital Specjalistyczny nr 4 w Bytomiu · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Transient tachypnea of the newborn (TTN), which results from inadequate absorption of fetal lung fluid, is the most common cause of neonatal respiratory distress. Stimulation of β-adrenergic receptors enhances alveolar fluid absorption. Therefore, the β2-adrenergic receptor agonist salbutamol has been proposed as a treatment for TTN. This study aims to evaluate the efficacy and safety of salbutamol as supportive pharmacotherapy together with non-invasive nasal continuous positive airway pressure (NIV/nCPAP) for the prevention of persistent pulmonary hypertension of the newborn (PPHN) in infants with TTN. Methods and analysis: This multicenter, double-blind, phase III trial will include infants with a gestational age between 32 and 42 weeks who are affected by respiratory disorders and treated in eight neonatal intensive care units in Poland. A total of 608 infants within 24 h after birth will be enrolled and randomly assigned (1:1) to receive nebulized salbutamol with NIV or placebo (nebulized 0.9% NaCl) with NIV. The primary outcome is the percentage of infants with TTN who develop PPHN. The secondary outcomes are the severity of respiratory distress (assessed with the modified TTN Silverman score), frequency of need for intubation, duration of NIV and hospitalization, acid-base balance (blood pH, partial pressure of O Discussion: The Respiratory Failure with Salbutamol (REFSAL) study will be the first clinical trial to evaluate the efficacy and safety of salbutamol in the prevention of persistent pulmonary hypertension in newborns with tachypnea, and will improve short term outcomes. If successful, the study will demonstrate the feasibility of early intervention with NIV/nCPAP together with nebulized salbutamol in the management of TTN. Ethics and dissemination: The study protocol was approved by the Bioethics Committee of the Medical University of Warsaw, Warsaw, Poland on November 16, 2020 (decision number KB/190/2020). All procedures will follow the principles of the Declaration of Helsinki. The results of the study will be submitted for knowledge translation in peer-reviewed journals and presented at national and international pediatric society conferences. Clinical Trial Registration: It is registered at ClinicalTrials.gov NCT05527704, EudraCT 2020-003913-36; Protocol version 5.0 from 04/01/2022.

Indexed as

neonatepersistent pulmonary hypertensionrespiratory distresssalbutamoltransient tachypnea

Identifiers

PMID36714639
PMCPMC9879660
OpenAlexW4315796280

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.