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. 2024 May 7;11(1):e002216.
doi: 10.1136/bmjresp-2023-002216.

Erdosteine in children and adults with bronchiectasis (BETTER trial): study protocol for a multicentre, double-blind, randomised controlled trial

Affiliations

Erdosteine in children and adults with bronchiectasis (BETTER trial): study protocol for a multicentre, double-blind, randomised controlled trial

Anne B Chang et al. BMJ Open Respir Res. .

Abstract

Introduction: Bronchiectasis is a worldwide chronic lung disorder where exacerbations are common. It affects people of all ages, but especially Indigenous populations in high-income nations. Despite being a major contributor to chronic lung disease, there are no licensed therapies for bronchiectasis and there remain relatively few randomised controlled trials (RCTs) conducted in children and adults. Our RCT will address some of these unmet needs by evaluating whether the novel mucoactive agent, erdosteine, has a therapeutic role in children and adults with bronchiectasis.Our primary aim is to determine in children and adults aged 2-49 years with bronchiectasis whether regular erdosteine over a 12-month period reduces acute respiratory exacerbations compared with placebo. Our primary hypothesis is that people with bronchiectasis who regularly use erdosteine will have fewer exacerbations than those receiving placebo.Our secondary aims are to determine the effect of the trial medications on quality of life (QoL) and other clinical outcomes (exacerbation duration, time-to-next exacerbation, hospitalisations, lung function, adverse events). We will also assess the cost-effectiveness of the intervention.

Methods and analysis: We are undertaking an international multicentre, double-blind, placebo-RCT to evaluate whether 12 months of erdosteine is beneficial for children and adults with bronchiectasis. We will recruit 194 children and adults with bronchiectasis to a parallel, superiority RCT at eight sites across Australia, Malaysia and Philippines. Our primary endpoint is the rate of exacerbations over 12 months. Our main secondary outcomes are QoL, exacerbation duration, time-to-next exacerbation, hospitalisations and lung function.

Ethics and dissemination: The Human Research Ethics Committees (HREC) of Children's Health Queensland (for all Australian sites), University of Malaya Medical Centre (Malaysia) and St. Luke's Medical Centre (Philippines) approved the study. We will publish the results and share the outcomes with the academic and medical community, funding and relevant patient organisations.

Trial registration number: ACTRN12621000315819.

Keywords: Bronchiectasis; Paediatric Lung Disaese.

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Conflict of interest statement

Competing interests: None declared.

Figures

Figure 1
Figure 1
Overall schematic study design of our randomised controlled trial. QoL, quality of life; RE, respiratory exacerbation.

References

    1. Chalmers JD, Chang AB, Chotirmall SH, et al. . Bronchiectasis. Nat Rev Dis Primers 2018;4:45. 10.1038/s41572-018-0042-3 - DOI - PubMed
    1. Chang AB, Fortescue R, Grimwood K, et al. . Task force report: European respiratory society guidelines for the management of children and adolescents with bronchiectasis. Eur Respir J 2021;58:2002990. 10.1183/13993003.02990-2020 - DOI - PubMed
    1. Chang AB, Zacharasiewicz A, Goyal V, et al. . Task force report: European respiratory society statement for defining respiratory exacerbations in children and adolescents with bronchiectasis for clinical trials. Eur Respir J 2022;60:2200300. 10.1183/13993003.00300-2022 - DOI - PubMed
    1. Chang AB, Masel JP, Boyce NC, et al. . Non-CF bronchiectasis-clinical and HRCT evaluation. Pediatric Pulmonology 2003;35:477–83. 10.1002/ppul.10289 - DOI - PubMed
    1. Laird P, Ball N, Brahim S, et al. . Prevalence of chronic respiratory diseases in aboriginal children: a whole population study. Pediatr Pulmonol 2022;57:3136–44. 10.1002/ppul.26148 - DOI - PMC - PubMed

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