Evidence map›Paper›PMID 33123558›Full record

ArticleERJ open research2020

Inhaled dry powder alginate oligosaccharide in cystic fibrosis: a randomised, double-blind, placebo-controlled, crossover phase 2b study.

Silke van Koningsbruggen-Rietschel, Jane C Davies, Tacjana Pressler, Rainald Fischer, Gordon MacGregor, Scott H Donaldson, Knut Smerud, Nils Meland, Jann Mortensen, Marie Ø Fosbøl and 4 more

Open access · goldAbstract read
In one paragraph

Article in ERJ open research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
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  3. Article
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  7. Mucin adhesion of serial cystic fibrosis airwaysFrontiers in cellular and infection microbiology · 2024
    Article
  8. Article
  9. Review
  10. How Three Self-Secreted Biofilm Exopolysaccharides ofInternational journal of molecular sciences · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Pseudomonas aeruginosa in the Cystic Fibrosis Lung.Advances in experimental medicine and biology · 2022
    Article
  16. What Is New in the Anti-Frontiers in cellular and infection microbiology · 2022
    Review
  17. Approaches to Targeting Bacterial Biofilms in Cystic Fibrosis Airways.International journal of molecular sciences · 2021
    Review
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

14 authors at 9 institutions in 5 countries.

Silke van Koningsbruggen-RietschelCF Centre, Faculty of Medicine, University Children's Hospital, Cologne, Germany.
Jane C DaviesDept of Paediatric Respiratory Medicine, National Heart and Lung Institute, Imperial College London, and Royal Brompton and Harefield NHS Foundation Trust, London, UK.
Tacjana PresslerCopenhagen CF Centre, Rigshospitalet, Copenhagen, Denmark.
Rainald FischerPneumologische Praxis Pasing, Munich, Germany.
Gordon MacGregorDept of Respiratory Medicine, Queen Elizabeth University Hospital, Glasgow, UK.
Scott H DonaldsonDept of Medicine, UNC School of Medicine, Chapel Hill, NC, USA.ORCID https://orcid.org/0000-0003-4802-0388
Knut SmerudSMERUD Medical Research International AS, Oslo, Norway.
Nils MelandSMERUD Medical Research International AS, Oslo, Norway.
Jann MortensenCopenhagen CF Centre, Rigshospitalet, Copenhagen, Denmark.
Marie Ø FosbølCopenhagen CF Centre, Rigshospitalet, Copenhagen, Denmark.
Damian G DowneyCentre for Experimental Medicine, Queen's University, Belfast, UK.
Astrid H MyrsetAlgiPharma AS, Sandvika, Norway.
Hugo FlatenAlgiPharma AS, Sandvika, Norway.
Philip D RyeAlgiPharma AS, Sandvika, Norway.ORCID https://orcid.org/0000-0001-7762-3300
AlgiPharma (Norway) · NORigshospitalet · DKSmerud Medical Research (Norway) · NOOrthopädische Praxis · DEQueen Elizabeth University Hospital · GBQueen's University Belfast · GBRoyal Brompton & Harefield NHS Foundation Trust · GBUniversity Hospital Cologne · DEUniversity of North Carolina Health Care · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOligoG is a low molecular-weight alginate oligosaccharide that improves the viscoelastic properties of cystic fibrosis (CF) mucus and disrupts biofilms, thereby potentiating the activity of antimicrobial agents. The efficacy of inhaled OligoG was evaluated in adult patients with CF.

methodsA randomised, double-blind, placebo-controlled multicentre crossover study was used to demonstrate safety and efficacy of inhaled dry powder OligoG. Subjects were randomly allocated to receive OligoG 1050 mg per day (10 capsules three times daily) or matching placebo for 28 days, with 28-day washout periods following each treatment period. The primary end-point was absolute change in percentage predicted forced expiratory volume in 1 s (FEV

resultsIn this study, 90 adult subjects were screened and 65 were randomised. Statistically significant improvement in FEV

conclusionsInhalation of OligoG-dry powder over 28 days was safe in adult CF subjects. Statistically significant improvement of FEV

Identifiers

PMID33123558
PMCPMC7569163
OpenAlexW3092705875

What OpenQuestion holds

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Registered trials

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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.