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A 2 × 2 factorial, randomised, open-label trial to determine the clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care over 52 weeks in adults with bronchiectasis: a protocol for the CLEAR clinical trial

BACKGROUND: Current guidelines for the management of bronchiectasis (BE) highlight the lack of evidence to recommend mucoactive agents, such as hypertonic saline (HTS) and carbocisteine, to aid sputum removal as part of standard care. We hypothesise that mucoactive agents (HTS or carbocisteine, or a...

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Autores principales: Bradley, Judy Martina, Anand, Rohan, O’Neill, Brenda, Ferguson, Kathryn, Clarke, Mike, Carroll, Mary, Chalmers, James, De Soyza, Anthony, Duckers, Jamie, Hill, Adam T., Loebinger, Michael R., Copeland, Fiona, Gardner, Evie, Campbell, Christina, Agus, Ashley, McGuire, Alistair, Boyle, Roisin, McKinney, Fionnuala, Dickson, Naomi, McAuley, Danny F., Elborn, Stuart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921594/
https://www.ncbi.nlm.nih.gov/pubmed/31856887
http://dx.doi.org/10.1186/s13063-019-3766-9
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author Bradley, Judy Martina
Anand, Rohan
O’Neill, Brenda
Ferguson, Kathryn
Clarke, Mike
Carroll, Mary
Chalmers, James
De Soyza, Anthony
Duckers, Jamie
Hill, Adam T.
Loebinger, Michael R.
Copeland, Fiona
Gardner, Evie
Campbell, Christina
Agus, Ashley
McGuire, Alistair
Boyle, Roisin
McKinney, Fionnuala
Dickson, Naomi
McAuley, Danny F.
Elborn, Stuart
author_facet Bradley, Judy Martina
Anand, Rohan
O’Neill, Brenda
Ferguson, Kathryn
Clarke, Mike
Carroll, Mary
Chalmers, James
De Soyza, Anthony
Duckers, Jamie
Hill, Adam T.
Loebinger, Michael R.
Copeland, Fiona
Gardner, Evie
Campbell, Christina
Agus, Ashley
McGuire, Alistair
Boyle, Roisin
McKinney, Fionnuala
Dickson, Naomi
McAuley, Danny F.
Elborn, Stuart
author_sort Bradley, Judy Martina
collection PubMed
description BACKGROUND: Current guidelines for the management of bronchiectasis (BE) highlight the lack of evidence to recommend mucoactive agents, such as hypertonic saline (HTS) and carbocisteine, to aid sputum removal as part of standard care. We hypothesise that mucoactive agents (HTS or carbocisteine, or a combination) are effective in reducing exacerbations over a 52-week period, compared to usual care. METHODS: This is a 52-week, 2 × 2 factorial, randomized, open-label trial to determine the clinical effectiveness and cost effectiveness of HTS 6% and carbocisteine for airway clearance versus usual care - the Clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care (CLEAR) trial. Patients will be randomised to (1) standard care and twice-daily nebulised HTS (6%), (2) standard care and carbocisteine (750 mg three times per day until visit 3, reducing to 750 mg twice per day), (3) standard care and combination of twice-daily nebulised HTS and carbocisteine, or (4) standard care. The primary outcome is the mean number of exacerbations over 52 weeks. Key inclusion criteria are as follows: adults with a diagnosis of BE on computed tomography, BE as the primary respiratory diagnosis, and two or more pulmonary exacerbations in the last year requiring antibiotics and production of daily sputum. DISCUSSION: This trial’s pragmatic research design avoids the significant costs associated with double-blind trials whilst optimising rigour in other areas of trial delivery. The CLEAR trial will provide evidence as to whether HTS, carbocisteine or both are effective and cost effective for patients with BE. TRIAL REGISTRATION: EudraCT number: 2017-000664-14 (first entered in the database on 20 October 2017). ISRCTN.com, ISRCTN89040295. Registered on 6 July/2018. Funder: National Institute for Health Research, Health Technology Assessment Programme (15/100/01). Sponsor: Belfast Health and Social Care Trust. Ethics Reference Number: 17/NE/0339. Protocol version: v3.0 Final_14052018.
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spelling pubmed-69215942019-12-30 A 2 × 2 factorial, randomised, open-label trial to determine the clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care over 52 weeks in adults with bronchiectasis: a protocol for the CLEAR clinical trial Bradley, Judy Martina Anand, Rohan O’Neill, Brenda Ferguson, Kathryn Clarke, Mike Carroll, Mary Chalmers, James De Soyza, Anthony Duckers, Jamie Hill, Adam T. Loebinger, Michael R. Copeland, Fiona Gardner, Evie Campbell, Christina Agus, Ashley McGuire, Alistair Boyle, Roisin McKinney, Fionnuala Dickson, Naomi McAuley, Danny F. Elborn, Stuart Trials Study Protocol BACKGROUND: Current guidelines for the management of bronchiectasis (BE) highlight the lack of evidence to recommend mucoactive agents, such as hypertonic saline (HTS) and carbocisteine, to aid sputum removal as part of standard care. We hypothesise that mucoactive agents (HTS or carbocisteine, or a combination) are effective in reducing exacerbations over a 52-week period, compared to usual care. METHODS: This is a 52-week, 2 × 2 factorial, randomized, open-label trial to determine the clinical effectiveness and cost effectiveness of HTS 6% and carbocisteine for airway clearance versus usual care - the Clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care (CLEAR) trial. Patients will be randomised to (1) standard care and twice-daily nebulised HTS (6%), (2) standard care and carbocisteine (750 mg three times per day until visit 3, reducing to 750 mg twice per day), (3) standard care and combination of twice-daily nebulised HTS and carbocisteine, or (4) standard care. The primary outcome is the mean number of exacerbations over 52 weeks. Key inclusion criteria are as follows: adults with a diagnosis of BE on computed tomography, BE as the primary respiratory diagnosis, and two or more pulmonary exacerbations in the last year requiring antibiotics and production of daily sputum. DISCUSSION: This trial’s pragmatic research design avoids the significant costs associated with double-blind trials whilst optimising rigour in other areas of trial delivery. The CLEAR trial will provide evidence as to whether HTS, carbocisteine or both are effective and cost effective for patients with BE. TRIAL REGISTRATION: EudraCT number: 2017-000664-14 (first entered in the database on 20 October 2017). ISRCTN.com, ISRCTN89040295. Registered on 6 July/2018. Funder: National Institute for Health Research, Health Technology Assessment Programme (15/100/01). Sponsor: Belfast Health and Social Care Trust. Ethics Reference Number: 17/NE/0339. Protocol version: v3.0 Final_14052018. BioMed Central 2019-12-19 /pmc/articles/PMC6921594/ /pubmed/31856887 http://dx.doi.org/10.1186/s13063-019-3766-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Bradley, Judy Martina
Anand, Rohan
O’Neill, Brenda
Ferguson, Kathryn
Clarke, Mike
Carroll, Mary
Chalmers, James
De Soyza, Anthony
Duckers, Jamie
Hill, Adam T.
Loebinger, Michael R.
Copeland, Fiona
Gardner, Evie
Campbell, Christina
Agus, Ashley
McGuire, Alistair
Boyle, Roisin
McKinney, Fionnuala
Dickson, Naomi
McAuley, Danny F.
Elborn, Stuart
A 2 × 2 factorial, randomised, open-label trial to determine the clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care over 52 weeks in adults with bronchiectasis: a protocol for the CLEAR clinical trial
title A 2 × 2 factorial, randomised, open-label trial to determine the clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care over 52 weeks in adults with bronchiectasis: a protocol for the CLEAR clinical trial
title_full A 2 × 2 factorial, randomised, open-label trial to determine the clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care over 52 weeks in adults with bronchiectasis: a protocol for the CLEAR clinical trial
title_fullStr A 2 × 2 factorial, randomised, open-label trial to determine the clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care over 52 weeks in adults with bronchiectasis: a protocol for the CLEAR clinical trial
title_full_unstemmed A 2 × 2 factorial, randomised, open-label trial to determine the clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care over 52 weeks in adults with bronchiectasis: a protocol for the CLEAR clinical trial
title_short A 2 × 2 factorial, randomised, open-label trial to determine the clinical and cost-effectiveness of hypertonic saline (HTS 6%) and carbocisteine for airway clearance versus usual care over 52 weeks in adults with bronchiectasis: a protocol for the CLEAR clinical trial
title_sort 2 × 2 factorial, randomised, open-label trial to determine the clinical and cost-effectiveness of hypertonic saline (hts 6%) and carbocisteine for airway clearance versus usual care over 52 weeks in adults with bronchiectasis: a protocol for the clear clinical trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6921594/
https://www.ncbi.nlm.nih.gov/pubmed/31856887
http://dx.doi.org/10.1186/s13063-019-3766-9
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