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用于酒精性肝炎的类固醇或己酮可可碱(STOPAH):一项随机对照试验的研究方案

Steroids or pentoxifylline for alcoholic hepatitis (STOPAH): study protocol for a randomised controlled trial.

作者信息

Forrest Ewan, Mellor Jane, Stanton Louise, Bowers Megan, Ryder Priscilla, Austin Andrew, Day Christopher, Gleeson Dermot, O'Grady John, Masson Steven, McCune Anne, Patch David, Richardson Paul, Roderick Paul, Ryder Stephen, Wright Mark, Thursz Mark

机构信息

Hepatology Section, Imperial College, Norfolk Place, London, Paddington W2 1NY, UK.

出版信息

Trials. 2013 Aug 19;14:262. doi: 10.1186/1745-6215-14-262.

Abstract

BACKGROUND

Alcoholic hepatitis is the most florid presentation of alcohol-related liver disease. In its severe form, defined by a Maddrey's discriminant function (DF) ≥32, the 28-day mortality rate is approximately 35%. A number of potential treatments have been subjected to clinical trials, of which two, corticosteroids and pentoxifylline, may have therapeutic benefit. The role of corticosteroids is controversial as trial results have been inconsistent, whereas the role of pentoxifylline requires confirmation as only one previous placebo-controlled trial has been published.

METHODS/DESIGN: STOPAH is a multicentre, double-blind, factorial (2 × 2) trial in which patients are randomised to one of four groups:1. Group A: placebo / placebo2. Group B: placebo / prednisolone3. Group C: pentoxifylline / placebo4. Group D: pentoxifylline / prednisoloneThe trial aims to randomise 1,200 patients with severe alcoholic hepatitis, in order to provide sufficient power to determine whether either of the two interventions is effective. The primary endpoint of the study is mortality at 28 days, with secondary endpoints being mortality at 90 days and 1 year.

DISCUSSION

STOPAH aims to be a definitive study to resolve controversy around the existing treatments for alcoholic hepatitis. Eligibility criteria are based on clinical parameters rather than liver biopsy, which are aligned with standard clinical practice in most hospitals. The use of a factorial design will allow two treatments to be evaluated in parallel, with efficient use of patient numbers to achieve high statistical power.

TRIAL REGISTRATION

EudraCT reference number: 2009-013897-42 ISRCTN reference number: ISRCTN88782125.

摘要

背景

酒精性肝炎是酒精相关肝病最典型的表现形式。其严重形式由马德雷判别函数(DF)≥32定义,28天死亡率约为35%。许多潜在治疗方法已进入临床试验,其中两种,即皮质类固醇和己酮可可碱,可能具有治疗益处。皮质类固醇的作用存在争议,因为试验结果不一致,而己酮可可碱的作用需要确认,因为此前仅发表过一项安慰剂对照试验。

方法/设计:STOPAH是一项多中心、双盲、析因(2×2)试验,患者被随机分为四组之一:

  1. A组:安慰剂/安慰剂

  2. B组:安慰剂/泼尼松龙

  3. C组:己酮可可碱/安慰剂

  4. D组:己酮可可碱/泼尼松龙

该试验旨在将1200例重症酒精性肝炎患者随机分组,以便有足够的效力来确定这两种干预措施是否有效。研究的主要终点是28天死亡率,次要终点是90天和1年死亡率。

讨论

STOPAH旨在成为一项确定性研究,以解决围绕酒精性肝炎现有治疗方法的争议。纳入标准基于临床参数而非肝活检,这与大多数医院的标准临床实践一致。采用析因设计将允许同时评估两种治疗方法,有效利用患者数量以实现高统计效力。

试验注册

欧洲临床试验数据库(EudraCT)参考编号:2009 - 013897 - 42 国际标准随机对照试验编号(ISRCTN):ISRCTN88782125

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