Evidence map›Paper›PMID 35534039›Full record

ArticleBMJ open respiratory research2022

Reducing exacerbations in children and adults with primary ciliary dyskinesia using erdosteine and/or azithromycin therapy (REPEAT trial): study protocol for a multicentre, double-blind, double-dummy, 2×2 partial factorial, randomised controlled trial.

Anne B Chang, Lucy C Morgan, Emma L Duncan, Mark D Chatfield, André Schultz, Paul J Leo, Gabrielle B McCallum, Aideen M McInerney-Leo, Steven M McPhail, Yuejen Zhao and 15 more

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in BMJ open respiratory research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 26% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Pulmonary exacerbations in primary ciliary dyskinesia.European journal of pediatrics · 2026
    Review
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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

25 authors at 8 institutions in 2 countries.

Anne B ChangChild Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia anne.chang@menzies.edu.au.ORCID 0000-0002-1331-3706
Lucy C MorganDepartment of Health and Ageing, Concord Repatriation General Hospital, Sydney, New South Wales, Australia.
Emma L DuncanSchool of Life Course & Population Sciences, King's College London, London, UK.
Mark D ChatfieldChild Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
André SchultzTelethon Kids Institute, University of Western Australia, Perth, Western Australia, Australia.
Paul J LeoAustralian Translational Genomics Centre, Queensland University of Technology, Brisbane, Queensland, Australia.
Gabrielle B McCallumChild Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Aideen M McInerney-LeoUniversity of Queensland Diamantina Institute, The University of Queensland, Brisbane, Queensland, Australia.
Steven M McPhailAustralian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.
Yuejen ZhaoChild Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Catherine KruljacPCD Australia Foundation, Melbourne, Victoria, Australia.
Heidi C Smith-VaughanChild Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Peter S MorrisChild Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Julie M MarchantAustralian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.
Stephanie T YerkovichChild Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Anne L CookAustralian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.
Danielle WurzelDepartment of Respiratory Medicine, Royal Children's Hospital, Melbourne, Victoria, Australia.
Lesley VersteeghChild Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Hannah O'FarrellChild Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Margaret S McElreaAustralian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.ORCID 0000-0001-9078-2357
Sabine FletcherAustralian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.
Heather D'AntoineChild Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
Enna Stroil-SalamaLung Foundation of Australia, Metro South Health, Brisbane, Queensland, Australia.
Phil J RobinsonDepartment of Respiratory Medicine, Royal Children's Hospital, Melbourne, Victoria, Australia.
Keith GrimwoodDepartments of Infectious Disease and Paediatrics, Gold Coast Health, Gold Coast, Queensland, Australia.
Queensland University of Technology · AUCharles Darwin University · AURoyal Children's Hospital · AUThe University of Queensland · AUConcord Repatriation General Hospital · AUGriffith University · AUQueensland Health · AUThe Kids Research Institute Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPrimary ciliary dyskinesia (PCD) is a rare, progressive, inherited ciliopathic disorder, which is incurable and frequently complicated by the development of bronchiectasis. There are few randomised controlled trials (RCTs) involving children and adults with PCD and thus evidence of efficacy for interventions are usually extrapolated from people with cystic fibrosis. Our planned RCT seeks to address some of these unmet needs by employing a currently prescribed (but unapproved for long-term use in PCD) macrolide antibiotic (azithromycin) and a novel mucolytic agent (erdosteine). The primary aim of our RCT is to determine whether regular oral azithromycin and erdosteine over a 12-month period reduces acute respiratory exacerbations among children and adults with PCD. Our primary hypothesis is that: people with PCD who regularly use oral azithromycin and/or erdosteine will have fewer exacerbations than those receiving the corresponding placebo medications. Our secondary aims are to determine the effect of the trial medications on PCD-specific quality-of-life (QoL) and other clinical outcomes (lung function, time-to-next exacerbation, hospitalisations) and nasopharyngeal bacterial carriage and antimicrobial resistance. METHODS AND ANALYSIS: We are currently undertaking a multicentre, double-blind, double-dummy RCT to evaluate whether 12 months of azithromycin and/or erdosteine is beneficial for children and adults with PCD. We plan to recruit 104 children and adults with PCD to a parallel, 2×2 partial factorial superiority RCT at five sites across Australia. Our primary endpoint is the rate of exacerbations over 12 months. Our main secondary outcomes are QoL, lung function and nasopharyngeal carriage by respiratory bacterial pathogens and their associated azithromycin resistance. ETHICS AND DISSEMINATION: Our RCT is conducted in accordance with Good Clinical Practice and the Australian legislation and National Health and Medical Research Council guidelines for ethical conduct of Research, including that for First Nations Australians. TRIAL REGISTRATION NUMBER: ACTRN12619000564156.

Indexed as

AzithromycinCiliary Motility DisordersAdultAustraliaChildEquivalence Trials as TopicHumansMulticenter Studies as TopicRandomized Controlled Trials as TopicThioglycolatesThiophenesAzithromycinerdosteineThioglycolatesThiophenesbronchiectasis

Identifiers

PMID35534039
PMCPMC9086630
OpenAlexW4280556552

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.