审计药物开发:临床试验方法的系统回顾。

IF 2.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Alcohol Pub Date : 2024-07-05 DOI:10.1016/j.alcohol.2024.06.007
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引用次数: 0

摘要

随着研究设计被证明会影响治疗效果,完善临床试验方法变得越来越重要。为了最大限度地提高随机临床试验(RCT)的效率,研究人员致力于建立标准化的实践方法。本系统性综述的目的是描述过去 40 年来酒精使用障碍(AUD)临床试验的方法实践。为实现这一目标,我们于 2023 年 4 月在 PubMed 上检索了 2018 年 7 月至 2023 年 4 月间发表的有关 AUD 药物的 RCT。搜索结果与之前从 1985 年到 2018 年的搜索结果相结合。纳入 RCT 研究的标准是(1) 随机对照试验;(2) 双盲或单盲;(3) 安慰剂或活性对照条件;(4) 以饮酒作为主要终点;(5) 4 周或更长时间的治疗;(6) 12 周或更长时间的随访。共总结了 139 项 RCT 的方法学数据,代表 19 种药物,时间跨度长达 40 年。结果显示,最常见的测试药物是纳曲酮(k=42)、阿坎普罗斯酸(k=24)和巴氯芬(k=11)。平均而言,参与者中 74% 为男性,随机前每月饮酒 226 次。治疗时间的中位数为 12 周(IQR= 12-16;最小值=4,最大值=52),随访时间的中位数为 12.5 周(IQR:12-26;最小值=7,最大值=104)。研究结果有两大领域(即戒酒和大量饮酒),大多数研究都包含这两个领域的结果(k=87;63%)。按年代对报告实践进行了总结,结果显示女性入选人数增加,种族和民族数据报告更好,要求审前禁欲的研究减少。本综述总结了针对 AUD 的随机临床试验的文献现状,包括单项研究的效应大小以及这组具有代表性的临床试验的主要方法学特征。
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Medication development for AUD: A systematic review of clinical trial methodology

Refining clinical trial methodology has become increasingly important as study design is shown to influence treatment efficacy. To maximize the efficiency of randomized clinical trials (RCTs), researchers aim to establish standardized practices. The goal of this systematic review is to describe methodological practices of clinical trials for alcohol use disorder (AUD) over the past 40 years. To achieve this goal, a PubMed search was conducted in April 2023 for RCTs on AUD medications published between July 2018 through April 2023. Resulting studies were combined with a previous search from 1985 through 2018. Inclusion criteria for the RCT studies were: (1) a randomized controlled trial, (2) double or single blinded, (3) placebo or active control condition, (4) alcohol use as the primary endpoint, (5) 4 or more weeks of treatment, and (6) 12 or more weeks of follow-up. In total, methodological data from 139 RCTs representing 19 medications and spanning the past four decades were summarized. Results indicated that the most common medications tested were naltrexone (k = 42), acamprosate (k = 24), and baclofen (k = 11). On average, participants were 74% male and consumed 226 drinks per month pre-randomization. The median length of treatment was 12 weeks (IQR = 12–16; min = 4 max = 52) and the median follow-up duration was 12.5 weeks (IQR: 12–26; min = 7 max = 104). There were two broad domains of outcomes (i.e., abstinence and heavy drinking), with most studies featuring outcomes from both domains (k = 87; 63%). Reporting practices were summarized by decade, revealing an increased enrollment of females, better reporting of race and ethnicity data, and less studies requiring pre-trial abstinence. This review summarizes the current state of the literature on randomized clinical trials for AUD including effect sizes for individual studies and summaries of key methodological features across this representative set of clinical trials.

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来源期刊
Alcohol
Alcohol 医学-毒理学
CiteScore
4.60
自引率
4.30%
发文量
74
审稿时长
15.6 weeks
期刊介绍: Alcohol is an international, peer-reviewed journal that is devoted to publishing multi-disciplinary biomedical research on all aspects of the actions or effects of alcohol on the nervous system or on other organ systems. Emphasis is given to studies into the causes and consequences of alcohol abuse and alcoholism, and biomedical aspects of diagnosis, etiology, treatment or prevention of alcohol-related health effects. Intended for both research scientists and practicing clinicians, the journal publishes original research on the neurobiological, neurobehavioral, and pathophysiological processes associated with alcohol drinking, alcohol abuse, alcohol-seeking behavior, tolerance, dependence, withdrawal, protracted abstinence, and relapse. In addition, the journal reports studies on the effects alcohol on brain mechanisms of neuroplasticity over the life span, biological factors associated with adolescent alcohol abuse, pharmacotherapeutic strategies in the treatment of alcoholism, biological and biochemical markers of alcohol abuse and alcoholism, pathological effects of uncontrolled drinking, biomedical and molecular factors in the effects on liver, immune system, and other organ systems, and biomedical aspects of fetal alcohol spectrum disorder including mechanisms of damage, diagnosis and early detection, treatment, and prevention. Articles are published from all levels of biomedical inquiry, including the following: molecular and cellular studies of alcohol''s actions in vitro and in vivo; animal model studies of genetic, pharmacological, behavioral, developmental or pathophysiological aspects of alcohol; human studies of genetic, behavioral, cognitive, neuroimaging, or pathological aspects of alcohol drinking; clinical studies of diagnosis (including dual diagnosis), treatment, prevention, and epidemiology. The journal will publish 9 issues per year; the accepted abbreviation for Alcohol for bibliographic citation is Alcohol.
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