Feasibility randomised multicentre, double-blind, double-dummy controlled trial of anakinra, an interleukin-1 receptor antagonist versus intramuscular methylprednisolone for acute gout attacks in patients with chronic kidney disease (ASGARD): protocol study

被引:6
作者
Balasubramaniam, Gowrie [1 ]
Parker, Trisha [2 ]
Turner, David [3 ]
Parker, Mike [2 ]
Scales, Jonathan [4 ]
Harnett, Patrick [1 ]
Harrison, Michael [2 ]
Ahmed, Khalid [5 ]
Bhagat, Sweta [6 ]
Marianayagam, Thiraupathy [7 ]
Pitzalis, Costantino [8 ]
Mallen, Christian [9 ]
Roddy, Edward [9 ]
Almond, Mike [1 ]
Dasgupta, Bhaskar [1 ]
机构
[1] Southend Univ Hosp NHS Fdn Trust, Dept Renal Med, Southend On Sea, Essex, England
[2] Anglia Ruskin Univ, Clin Trials Unit, Bishops Hall Lane, Chelmsford, Essex, England
[3] Univ East Anglia, Norwich Med Sch, Norwich, Norfolk, England
[4] Univ Essex, Sch Hlth & Human Sci, Wivenhoe Pk, Colchester, Essex, England
[5] Princess Alexandria Hosp NHS Trust, Harlow, Essex, England
[6] West Suffolk Hosp NHS Fdn Trust, Bury St Edmunds, Suffolk, England
[7] East & North Herfordshire NHS Trust, Lister Hosp, Corey Mills Lane, Stevenage, Herts, England
[8] William Harvey Res Inst, Barts & London, Ctr Expt Med & Rheumatol, London, England
[9] Keele Univ, Primary Care & Hlth Sci, Keele, Staffs, England
基金
美国国家卫生研究院;
关键词
PLACEBO-CONTROLLED TRIAL; RHEUMATOID-ARTHRITIS; AMERICAN-COLLEGE; REFRACTORY GOUT; RENAL-FUNCTION; MANAGEMENT; CANAKINUMAB; THERAPY; FLARES; RISK;
D O I
10.1136/bmjopen-2017-017121
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Acute gout occurs in people with chronic kidney disease, who are commonly older people with comorbidities such as hypertension, heart disease and diabetes. Potentially harmful treatments are administered to these vulnerable patients due to a lack of clear evidence. Newly available treatment that targets a key inflammatory pathway in acute gout attacks provides an opportunity to undertake the first-ever trial specifically looking treating people with kidney disease. This paper describes the protocol for a feasibility randomised controlled trial (RCT) comparing anakinra, a novel interleukin-1 antagonist versus steroids in people with chronic kidney disease (ASGARD). Methods and analysis ASGARD is a two-parallel group double-blind, double-dummy multicentre RCT comparing anakinra 100 mg, an interleukin-1 antagonist, subcutaneous for 5 days against intramuscular methylprednisolone 120 mg. The primary objective is to assess the feasibility of the trial design and procedures for a definitive RCT. The specific aims are: (1) test recruitment and retention rates and willingness to be randomised; (2) test eligibility criteria; (3) collect and analyse outcome data to inform sample and power calculations for a trial of efficacy; (4) collect economic data to inform a future economic evaluation estimating costs of treatment and (5) assess capacity of the project to scale up to a national multicentre trial. We will also gather qualitative insights from participants. It aims to recruit 32 patients with a 1: 1 randomisation. Information from this feasibility study will help design a definitive trial and provide general information in designing acute gout studies. Ethics and dissemination The London-Central Ethics Committee approved the protocol. The results will be disseminated in peer-reviewed journals and at scientific conferences.
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页数:11
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