4.4 Article

Citalopram for treatment of cocaine use disorder: A Bayesian drop-the-loser randomized clinical trial

期刊

DRUG AND ALCOHOL DEPENDENCE
卷 228, 期 -, 页码 -

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.drugalcdep.2021.109054

关键词

Cocaine use disorder; Citalopram; Drop-the-loser; Bayesian adaptive design; Randomized clinical trial

资金

  1. NIDA [P50 DA009262-20]

向作者/读者索取更多资源

The study compared two doses of citalopram (20 mg and 40 mg) with placebo in terms of cocaine abstinence duration, with the 40 mg dose showing moderate-to-strong evidence for positive effects on both abstinence duration and cocaine-negative urine drug screens. The 40 mg dose was declared the winner in this drop-the-loser trial.
Background: Medication development research for cocaine use disorder (CUD) has been a longstanding goal in addiction research, but has not resulted in an FDA-approved treatment. Rising cocaine use rates underscore the need for efficient adaptive designs. This study compared differences between two doses of the selective serotonin reuptake inhibitor (SSRI) citalopram (versus placebo) on duration of cocaine abstinence and applied adaptive decision rules to select the 'best efficacy' dose. Methods: A double-blind, placebo-controlled, randomized Bayesian drop-the-loser (DTL) trial with three arms compared placebo to citalopram 20 mg and 40 mg. Adults (N = 107) with CUD attended thrice-weekly clinic visits for 9 weeks. The primary outcome was longest duration of abstinence (LDA), based on continuous cocaine negative urine drug screens (UDS). The secondary outcome was probability of cocaine-negative UDS during treatment. A planned interim analysis performed at approximately 50% of recruitment dropped the least effective active medication. Bayesian inference was used for all analyses with a pre-specified posterior probability (PP) threshold PP >= 95% considered statistically reliable evidence Results: Citalopram 40 mg satisfied interim efficacy criteria and was retained for the second half of the trial. For LDA, analyses indicated PP = 82% and PP = 65% of benefit for 40 mg and 20 mg, respectively (each relative to placebo). The odds of having cocaine-negative UDS decreased in all groups over 9 weeks but remained higher for 40 mg (PP = 97.4%) Conclusions: Neither dose met the 95% PP threshold for the primary outcome; however, 40 mg provided moderate-to-strong evidence for positive effects on LDA and cocaine-negative UDS. The 40 mg dose was declared the winner in this DTL trial.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.4
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据