Evidence map›Paper›PMID 42769362›Full record

ArticleERJ open research2026

Effects of hypertonic saline and/or carbocisteine on sputum rheology in bronchiectasis: CLEAR-EME.

Michael C McKelvey, Gisli G Einarsson, Jack Carson, Aram Kadoom, Ryan R Brown, Christina Campbell, Andrew Jackson, Cliona McDowell, Mike Clarke, Fiona Copeland and 24 more

Abstract read
In one paragraph

Article in ERJ open research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

34 authors.

Michael C McKelveyWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
Gisli G EinarssonSchool of Pharmacy, Queen's University Belfast, Belfast, UK.
Jack CarsonSchool of Pharmacy, Queen's University Belfast, Belfast, UK.
Aram KadoomSchool of Pharmacy, Queen's University Belfast, Belfast, UK.
Ryan R BrownWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
Christina CampbellNorthern Ireland Clinical Trials Unit, Belfast Health and Social Care Trust, Belfast, UK.
Andrew JacksonNorthern Ireland Clinical Trials Unit, Belfast Health and Social Care Trust, Belfast, UK.
Cliona McDowellNorthern Ireland Clinical Trials Unit, Belfast Health and Social Care Trust, Belfast, UK.
Mike ClarkeNorthern Ireland Clinical Trials Unit, Belfast Health and Social Care Trust, Belfast, UK.
Fiona CopelandPrimary Ciliary Dyskinesia Family Support Group, Ciliopathy Alliance, London, UK.
Kathryn FergusonWestern Health and Social Care Trust, Londonderry, UK.
Rebecca H McLeeseWellcome Trust-Wolfson Northern Ireland Clinical Research Facility, Queen's University Belfast, Belfast, UK.ORCID https://orcid.org/0000-0003-0647-2503
Rory ConverySouthern Health and Social Care Trust, Craigavon, UK.
Adam T HillDepartment of Respiratory Medicine, Centre for Inflammation Research, University of Edinburgh, Edinburgh, UK.
Anthony De SoyzaPopulation Health Sciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle, UK.ORCID https://orcid.org/0000-0002-8566-0344
Mitra ShahidiBuckingham Healthcare NHS Trust, Amersham, UK.
Martin KellyWestern Health and Social Care Trust, Londonderry, UK.
Mary CarrollUniversity Hospital Southampton NHS Foundation Trust, Southampton, UK.
Timothy GatheralDepartment of Respiratory Medicine, University Hospitals of Morecambe Bay NHS Foundation Trust, Morecambe Bay, UK.
Muhammed AnwarPrincess Alexandra Hospital, Harlow, UK.
Jamie DuckersUniversity Hospital Llandough Cardiff and Vale University Health Board, Cardiff, UK.ORCID https://orcid.org/0000-0003-3004-279X
William FlightOxford University Hospitals NHS Foundation Trust, Oxford, UK.
John R HurstUCL Respiratory, University College London, London, UK.ORCID https://orcid.org/0000-0002-7246-6040
A Alina IonescuRoyal Gwent Hospital, Newport, UK.
Michael R LoebingerRoyal Brompton Hospital, London, UK.
Anita L SullivanUniversity Hospitals Birmingham, Birmingham, UK.
James D ChalmersScottish Centre for Respiratory Research, Ninewells Hospital and Medical School, University of Dundee, Dundee, UK.
Damian G DowneyWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
Michael M TunneySchool of Pharmacy, Queen's University Belfast, Belfast, UK.
Brenda O'NeillInstitute of Nursing and Health Research, Ulster University, Belfast, UK.
Daniel F McAuleyWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.ORCID https://orcid.org/0000-0002-3283-1947
J Stuart ElbornWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
Judy M BradleyWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.
Clifford C TaggartWellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, UK.

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background: Mucoactives such as hypertonic saline (HTS) and carbocisteine are widely used in the treatment of bronchiectasis, though there is insufficient evidence to support their use. The aim of this mechanistic sub-study, embedded within the CLEAR trial, was to characterise the properties of sputum from patients with bronchiectasis and to assess whether treatment with HTS and/or carbocisteine altered these properties. Methods: In CLEAR, patients were randomised to receive HTS, carbocisteine, HTS plus carbocisteine or standard care, and sputum samples were collected at randomisation (baseline) and at 2 and 8 weeks post-randomisation. Sputum viscoelasticity was determined by rotational plate rheometry. Biomarkers were quantified by ELISA and microbiome composition was assessed by next-generation sequencing. The primary outcome was differences in sputum viscoelasticity between groups at 2 weeks following the commencement of treatment. Results: Sputum viscoelastic properties were not reduced by 2 or 8 weeks of treatment with HTS and/or carbocisteine (n=6-15 per group). Sputum biomarker levels and bacterial community composition were similar across groups at 2 or 8 weeks. At baseline, viscoelasticity (crossover point σ Conclusions: These data do not support the use of HTS or carbocisteine to alter sputum viscoelasticity, inflammatory marker levels or bacterial community composition in patients with bronchiectasis.

Identifiers

PMID42769362
PMCPMC13591285

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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.