Your browser doesn't support javascript.
loading
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.
Chang, Anne B; Morgan, Lucy C; Duncan, Emma L; Chatfield, Mark D; Schultz, André; Leo, Paul J; McCallum, Gabrielle B; McInerney-Leo, Aideen M; McPhail, Steven M; Zhao, Yuejen; Kruljac, Catherine; Smith-Vaughan, Heidi C; Morris, Peter S; Marchant, Julie M; Yerkovich, Stephanie T; Cook, Anne L; Wurzel, Danielle; Versteegh, Lesley; O'Farrell, Hannah; McElrea, Margaret S; Fletcher, Sabine; D'Antoine, Heather; Stroil-Salama, Enna; Robinson, Phil J; Grimwood, Keith.
Affiliation
  • Chang AB; Child 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.
  • Morgan LC; Australian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.
  • Duncan EL; Department of Respiratory Medicine, Queensland Children's Hospital, Brisbane, Queensland, Australia.
  • Chatfield MD; Department of Health and Ageing, Concord Repatriation General Hospital, Sydney, New South Wales, Australia.
  • Schultz A; School of Life Course & Population Sciences, King's College London, London, UK.
  • Leo PJ; Department of Endocrinology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • McCallum GB; Australian Translational Genomics Centre, Queensland University of Technology, Brisbane, Queensland, Australia.
  • McInerney-Leo AM; Child Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
  • McPhail SM; Faculty of Medicine, The University of Queensland, Brisbane, Queensland, Australia.
  • Zhao Y; Telethon Kids Institute, University of Western Australia, Perth, Western Australia, Australia.
  • Kruljac C; Department of Respiratory and Sleep Medicine, Perth Children's Hospital, Perth, Western Australia, Australia.
  • Smith-Vaughan HC; Australian Translational Genomics Centre, Queensland University of Technology, Brisbane, Queensland, Australia.
  • Morris PS; Child Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
  • Marchant JM; University of Queensland Diamantina Institute, The University of Queensland, Brisbane, Queensland, Australia.
  • Yerkovich ST; Australian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.
  • Cook AL; Child Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
  • Wurzel D; Health Gains Planning, Northern Territory Department of Health, Darwin, Northern Territory, Australia.
  • Versteegh L; PCD Australia Foundation, Melbourne, Victoria, Australia.
  • O'Farrell H; Child Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
  • McElrea MS; Child Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
  • Fletcher S; Australian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.
  • D'Antoine H; Department of Respiratory Medicine, Queensland Children's Hospital, Brisbane, Queensland, Australia.
  • Stroil-Salama E; Child Health Division and NHMRC Centre for Research Excellence in Paediatric Bronchiectasis (AusBREATHE), Menzies School of Health Research, Charles Darwin University, Darwin, Northern Territory, Australia.
  • Robinson PJ; Australian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.
  • Grimwood K; Australian Centre for Health Services Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.
BMJ Open Respir Res ; 9(1)2022 05.
Article in En | MEDLINE | ID: mdl-35534039
INTRODUCTION: Primary 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.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ciliary Motility Disorders / Azithromycin Type of study: Clinical_trials / Guideline Aspects: Ethics / Patient_preference Limits: Adult / Child / Humans Country/Region as subject: Oceania Language: En Journal: BMJ Open Respir Res Year: 2022 Document type: Article Affiliation country: Australia Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Ciliary Motility Disorders / Azithromycin Type of study: Clinical_trials / Guideline Aspects: Ethics / Patient_preference Limits: Adult / Child / Humans Country/Region as subject: Oceania Language: En Journal: BMJ Open Respir Res Year: 2022 Document type: Article Affiliation country: Australia Country of publication: United kingdom