Evidence map›Paper›PMID 25872649›Full record

Trial reportTrials2015

Pain reduction with oral methotrexate in knee osteoarthritis, a pragmatic phase iii trial of treatment effectiveness (PROMOTE): study protocol for a randomized controlled trial.

Sarah R Kingsbury, Puvan Tharmanathan, Nigel K Arden, Michael Batley, Fraser Birrell, Kim Cocks, Michael Doherty, Chris J Edwards, Toby Garrood, Andrew J Grainger and 10 more

Open access · goldAbstract readClinical Trial, Phase IIIMulticenter StudyPragmatic Clinical Trial
In one paragraph

Trial report in Trials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
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  6. Article
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  9. Review
  10. Review
  11. Article
  12. Article
  13. Macrophages in osteoarthritis: pathophysiology and therapeutics.American journal of translational research · 2020
    Article
  14. Review
  15. Article
  16. Update on novel pharmacological therapies for osteoarthritis.Therapeutic advances in musculoskeletal disease · 2019
    Review
  17. New Drug Treatments for Osteoarthritis: What is on the Horizon?European medical journal. Rheumatology · 2017
    Article
  18. Article
  19. 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

20 authors at 16 institutions in 1 country.

Sarah R KingsburyLeeds Institute of Rheumatic and Musculoskeletal Medicine and National Institute of Health Research (NIHR) Leeds Musculoskeletal Biomedical Research Unit, University of Leeds, Chapeltown Road, Leeds, LS7 4SA, UK. s.r.kingsbury@leeds.ac.uk.
Puvan TharmanathanYork Trials Unit, Department of Health Sciences, Faculty of Science, Seebohm Rowntree Building, University of York, Heslington, York, YO10 5DD, UK. puvan.nathan@york.ac.uk.
Nigel K ArdenNIHR Musculoskeletal Biomedical Research Unit, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Orthopaedic Centre, University of Oxford, Windmill Road, Headington, Oxford, OX3 7LD, UK. nigel.arden@ndorms.ox.ac.uk.
Michael BatleyDepartment of Rheumatology, Maidstone and Tunbridge Wells NHS Trust, Pembury, Tunbridge Wells, Kent, TN2 4QJ, UK. mbatley@nhs.net.
Fraser BirrellMusculoskeletal Research Group, Institute for Cellular Medicine, Newcastle University, Musculoskeletal Research Group, 4th Floor Catherine Cookson Building, The Medical School, Framlington Place, Newcastle University, Newcastle, NE2 4HH, UK. Fraser.Birrell@newcastle.ac.uk.
Kim CocksYork Trials Unit, Department of Health Sciences, Faculty of Science, Seebohm Rowntree Building, University of York, Heslington, York, YO10 5DD, UK. kim.cocks@york.ac.uk.
Michael DohertyAcademic Rheumatology, Clinical Sciences Building, University of Nottingham, Nottingham City Hospital, Hucknall Road, Nottingham, NG5 1 PB, UK. Michael.doherty@nottingham.ac.uk.
Chris J EdwardsDepartment of Rheumatology and NIHR Wellcome Trust Clinical Research Facility, University Hospital Southampton NHS Foundation Trust, Southampton, SO16 6YD, UK. cedwards@soton.ac.uk.
Toby GarroodGuy's and St Thomas' Hospitals Foundation NHS Trust, Great Maze Pond, London, SE1 9RT, UK. toby.garrood@gstt.nhs.uk.
Andrew J GraingerLeeds Institute of Rheumatic and Musculoskeletal Medicine and National Institute of Health Research (NIHR) Leeds Musculoskeletal Biomedical Research Unit, University of Leeds, Chapeltown Road, Leeds, LS7 4SA, UK. andrewgrainger@nhs.net.
Michael GreenThe York Hospital, York Hospitals NHS Foundation Trust, Wigginton Road, York, YO31 8HE, UK. Michael.Green@york.nhs.uk.
Catherine HewittYork Trials Unit, Department of Health Sciences, Faculty of Science, Seebohm Rowntree Building, University of York, Heslington, York, YO10 5DD, UK. catherine.hewitt@york.ac.uk.
Rod HughesRheumatology Department, St Peters Hospital, Guildford Road, Chertsey, Surrey, KT16 0PZ, UK. Rod.Hughes@asph.nhs.uk.
Robert MootsInstitute of Integrative Biology, University of Liverpool and Institute of Ageing and Chronic Disease, University Hospital Aintree, Longmoor Lane, Fazakerley, Liverpool, Merseyside, L9 7AL, UK. R.J.Moots@liverpool.ac.uk.
Terence W O'NeillArthritis Research UK Centre for Epidemiology, The University of Manchester, 2nd floor, Stopford Building, Oxford Road, Manchester, M13 9PT, UK. terence.oneill@manchester.ac.uk.
Edward RoddyResearch Institute for Primary Care and Health Sciences, Keele University, Keele, Staffordshire, ST5 5BG, UK. e.roddy@keele.ac.uk.
David L ScottDepartment of Rheumatology, King's College London School of Medicine, King's College London and Department of Rheumatology, King's College Hospital, 10 Cutcombe Road, London SE5 9RJ, London, UK. d.scott1@nhs.net.
Fiona E WattKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Windmill Road, Oxford, OX3 7HE, UK and Imperial College London, South Kensington Campus, London, SW7 2AZ, UK. fiona.watt@kennedy.ox.ac.uk.
David J TorgersonYork Trials Unit, Department of Health Sciences, Faculty of Science, Seebohm Rowntree Building, University of York, Heslington, York, YO10 5DD, UK. david.torgerson@york.ac.uk.
Philip G ConaghanLeeds Institute of Rheumatic and Musculoskeletal Medicine and National Institute of Health Research (NIHR) Leeds Musculoskeletal Biomedical Research Unit, University of Leeds, Chapeltown Road, Leeds, LS7 4SA, UK. p.conaghan@leeds.ac.uk.
University of York · GBUniversity of Leeds · GBGuy's and St Thomas' NHS Foundation Trust · GBImperial College London · GBKeele University · GBKing's College London · GBMaidstone and Tunbridge Wells NHS Trust · GBNewcastle University · GBNIHR Leeds Musculoskeletal Biomedical Research Unit · GBNottingham City Hospital · GBSt Peter's Hospital · GBUniversity Hospital Southampton NHS Foundation Trust · GBUniversity of Liverpool · GBUniversity of Manchester · GBUniversity of Oxford · GBYork Hospital · GB

Funding

Arthritis Research UK 20186Medical Research Council MR/K006312/1Medical Research Council MR/L01629X/1Versus Arthritis 20186
6 · The paper itself

Abstract

backgroundOsteoarthritis (OA) is the fastest growing cause of disability worldwide. Current treatments for OA are severely limited and a large proportion of people with OA live in constant, debilitating pain. There is therefore an urgent need for novel treatments to reduce pain. Synovitis is highly prevalent in OA and is associated with pain. In inflammatory arthritides such as rheumatoid arthritis, methotrexate (MTX) is the gold standard treatment for synovitis and has a well-known, acceptable toxicity profile. We propose that using MTX to treat patients with symptomatic knee OA will be a practical and safe treatment to reduce synovitis and, consequently, pain. METHODS/

designPain Reduction with Oral Methotrexate in knee Osteoarthritis, a pragmatic phase III trial of Treatment Effectiveness (PROMOTE) is an investigator-initiated, multi-centre, randomized, double-blind, pragmatic placebo-controlled trial. A total of 160 participants with symptomatic knee OA will be recruited across primary and secondary care sites in the United Kingdom and randomized on a 1:1 basis to active treatment or placebo, in addition to usual care, for 12 months. As is usual practice for MTX, dosing will be escalated over six weeks to 25 mg (or maximum tolerated dose) weekly for the remainder of the study. The primary endpoint is change in average knee pain during the past week (measured on an 11-point numerical rating scale) between baseline and six months. Secondary endpoints include other self-reported pain, function and quality-of-life measures. A health economics analysis will also be performed. A magnetic resonance imaging substudy will be conducted to provide an explanatory mechanism for associated symptom change by examining whether MTX reduces synovitis and whether this is related to symptom change. Linear and logistic regression will be used to compare changes between groups using univariable and multivariable modelling analyses. All analyses will be conducted on an intention-to-treat basis. DISCUSSION: The PROMOTE trial is designed to examine whether MTX is an effective analgesic treatment for OA. The MRI substudy will address the relationship between synovitis and symptom change. This will potentially provide a much needed new treatment for knee OA.

trial registrationCurrent Controlled Trials identifier: ISRCTN77854383 (registered: 25 October 2013).

Indexed as

Administration, OralAnalgesicsAnti-Inflammatory AgentsArthralgiaClinical ProtocolsDouble-Blind MethodHumansIntention to Treat AnalysisLinear ModelsLogistic ModelsMagnetic Resonance ImagingMethotrexateMultivariate AnalysisOsteoarthritis, KneePain MeasurementResearch DesignAnalgesicsAnti-Inflammatory AgentsMethotrexate

Identifiers

PMID25872649
PMCPMC4351849
OpenAlexW2160745547

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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.