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

被引:31
|
作者
Kingsbury, Sarah R. [1 ,2 ]
Tharmanathan, Puvan [3 ]
Arden, Nigel K. [4 ]
Batley, Michael [5 ]
Birrell, Fraser [6 ]
Cocks, Kim [3 ]
Doherty, Michael [7 ]
Edwards, Chris J. [8 ,9 ]
Garrood, Toby [10 ]
Grainger, Andrew J. [1 ,2 ]
Green, Michael [11 ]
Hewitt, Catherine [3 ]
Hughes, Rod [12 ]
Moots, Robert [13 ,14 ]
O'Neill, Terence W. [15 ]
Roddy, Edward [16 ]
Scott, David L. [17 ,18 ]
Watt, Fiona E. [19 ,20 ]
Torgerson, David J. [3 ]
Conaghan, Philip G. [1 ,2 ]
机构
[1] Univ Leeds, Leeds Inst Rheumat & Musculoskeletal Med, Leeds LS7 4SA, W Yorkshire, England
[2] Univ Leeds, NIHR Leeds Musculoskeletal Biomed Res Unit, Leeds LS7 4SA, W Yorkshire, England
[3] Univ York, Fac Sci, Dept Hlth Sci, York Trials Unit, York YO10 5DD, N Yorkshire, England
[4] Univ Oxford, NIHR Musculoskeletal Biomed Res Unit, Nuffield Dept Orthopaed Rheumatol & Musculoskelet, Nuffield Orthopaed Ctr, Oxford OX3 7LD, England
[5] Maidstone & Tunbridge Wells NHS Trust, Dept Rheumatol, Tunbridge Wells TN2 4QJ, Kent, England
[6] Newcastle Univ, Sch Med, Musculoskeletal Res Grp, Inst Cellular Med, Newcastle Upon Tyne NE2 4HH, Tyne & Wear, England
[7] Univ Nottingham, City Hosp Nottingham, Acad Rheumatol, Nottingham NG5 1PB, England
[8] Univ Hosp Southampton NHS Fdn Trust, Dept Rheumatol, Southampton SO16 6YD, Hants, England
[9] Univ Hosp Southampton NHS Fdn Trust, NIHR Wellcome Trust Clin Res Facil, Southampton SO16 6YD, Hants, England
[10] Guys & St Thomas Hosp Fdn NHS Trust, London SE1 9RT, England
[11] York Hosp NHS Fdn Trust, York Hosp, York YO31 8HE, N Yorkshire, England
[12] St Peters Hosp, Rheumatol Dept, Chertsey KT16 0PZ, Surrey, England
[13] Univ Liverpool, Inst Integrat Biol, Liverpool L9 7AL, Merseyside, England
[14] Aintree Univ Hosp NHS Fdn Trust, Inst Ageing & Chron Dis, Liverpool L9 7AL, Merseyside, England
[15] Univ Manchester, Arthrit Res UK Ctr Epidemiol, Manchester M13 9PT, Lancs, England
[16] Keele Univ, Res Inst Primary Care & Hlth Sci, Keele ST5 5BG, Staffs, England
[17] Kings Coll London, Sch Med, Dept Rheumatol, London SE5 9RJ, England
[18] Kings Coll Hosp London, Dept Rheumatol, London SE5 9RJ, England
[19] Univ Oxford, Kennedy Inst Rheumatol, Nuffield Dept Orthopaed Rheumatol & Musculoskelet, Oxford OX3 7HE, England
[20] Univ London Imperial Coll Sci Technol & Med, London SW7 2AZ, England
关键词
Double-blind; Knee osteoarthritis; Methotrexate; Placebo-controlled; Randomized; LOW-DOSE METHOTREXATE; RHEUMATOID-ARTHRITIS; CLINICAL-TRIALS; SYSTEMATIC ANALYSIS; SYNOVIAL-MEMBRANE; OUTCOME DOMAINS; GLOBAL BURDEN; PART; DISEASE; CARTILAGE;
D O I
10.1186/s13063-015-0602-8
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Osteoarthritis (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/Design: Pain 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.
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页数:14
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