Benzodiazepine agonist treatment for patients with benzodiazepine dependence undergoing opioid agonist treatment: a study protocol for the randomized controlled trial BMX-BAR.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2025-01-02 DOI:10.1186/s13063-024-08692-8
Fatemeh Chalabianloo, Lars Thore Fadnes, Jörg Assmus, Jon Mordal, Kristin K Solli, Kjetil S Dale, Christina D Andersen, Silvia Zavenova, Beathe H Rønning, Andreas W Blomkvist, Martin Ryssdal, Wasifa S J Butt, Anne Marciuch, Anne G Ørmen, Christian Ohldieck, Else-Marie Løberg, Kjell Arne Johansson
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引用次数: 0

Abstract

Background: There is a lack of knowledge on effective treatment methods for comorbid benzodiazepine dependence in populations undergoing opioid agonist treatment (OAT). Tapering and discontinuation of benzodiazepines has long been considered the standard treatment, even though there is limited evidence for this practice. There is also limited research on benzodiazepine agonist treatment; however, peer and clinical experiences indicate that such approaches may be beneficial for a subgroup of the patients with long-lasting benzodiazepine dependence not responding to other treatment approaches. A randomized controlled trial will be conducted to compare the efficacy and safety of stabilizing agonist treatment using prescribed benzodiazepines with standard treatment in reducing illicit benzodiazepine use.

Methods: The target sample is 108 participants at outpatient OAT clinics in six Norwegian cities/counties (Bergen/Vestland, Tønsberg/Vestfold, Skien/Telemark, Fredrikstad/Østfold, Tromsø/Troms, and Lillestrøm/Akershus). The main inclusion criteria are benzodiazepine dependence of ≥ 5 years, using ≥ 5 days a week during the last month, and previous attempts at tapering. Participants will be randomly assigned to receive either a 26-week benzodiazepine stabilizing treatment (15-30 mg diazepam or 50-100 mg oxazepam daily), or a 20-week tapering using the same medications and equivalent initial dosages. All participants will be given access to consultations from OAT therapists with psychosocial follow-up in accordance with current clinical practice. The primary outcome is the use of illicit benzodiazepines assessed by observed urinary tests at week 24. Secondary outcomes include mental health symptoms, quality of life, cognitive performance, violence risk, other substance use, treatment retention, and life satisfaction. Additionally, the study will assess treatment-related adverse events as well as the cost-effectiveness of the intervention.

Discussion: This is the first randomized controlled trial of benzodiazepine agonist treatment for benzodiazepine dependence. The research project will assess efficacy and safety of stabilizing treatment with prescribed benzodiazepines compared to benzodiazepine tapering and discontinuation regarding use of illicit benzodiazepines and accordingly well-being of patients with concurrent benzodiazepine and opioid dependence undergoing OAT. If the intervention is found to be efficacious and safe, it will be considered one of the options to standard treatment for this patient group.

Trial registration: EU trial number: EudraCT: 2021-004981-37. Registered on December 13, 2021.

接受阿片类激动剂治疗的苯二氮卓类药物依赖患者的苯二氮卓类激动剂治疗:BMX-BAR随机对照试验的研究方案
背景:在接受阿片激动剂治疗(OAT)的人群中,对苯二氮卓类药物共病依赖的有效治疗方法缺乏了解。逐渐减少和停用苯二氮卓类药物一直被认为是标准的治疗方法,尽管这种做法的证据有限。关于苯二氮卓类激动剂治疗的研究也很有限;然而,同行和临床经验表明,这种方法可能有利于长期苯二氮卓类药物依赖的亚组患者对其他治疗方法没有反应。将进行一项随机对照试验,比较使用处方苯二氮卓类药物稳定激动剂治疗与标准治疗在减少非法苯二氮卓类药物使用方面的有效性和安全性。方法:目标样本为挪威6个城市/县(卑尔根/Vestland、Tønsberg/Vestfold、Skien/Telemark、Fredrikstad/Østfold、trom瑟/Troms和Lillestrøm/Akershus) OAT门诊诊所的108名参与者。主要纳入标准为苯二氮卓类药物依赖≥5年,最近一个月每周使用≥5天,既往尝试过逐渐减少。参与者将被随机分配接受为期26周的苯二氮卓类稳定治疗(每天15-30毫克地西泮或50-100毫克奥西泮),或使用相同药物和相同初始剂量的20周逐渐减少。所有参与者将获得OAT治疗师的咨询,并根据当前的临床实践进行心理社会随访。主要结果是在第24周通过观察尿液测试评估非法苯二氮卓类药物的使用情况。次要结局包括精神健康症状、生活质量、认知能力、暴力风险、其他物质使用、治疗保留和生活满意度。此外,该研究将评估与治疗相关的不良事件以及干预的成本效益。讨论:这是首个苯二氮卓类激动剂治疗苯二氮卓类药物依赖的随机对照试验。该研究项目将评估处方苯二氮卓类药物稳定治疗的有效性和安全性,与苯二氮卓类药物逐渐减少和停止使用非法苯二氮卓类药物相比,以及同时存在苯二氮卓类药物和阿片类药物依赖的患者在OAT中的健康状况。如果发现干预措施是有效和安全的,它将被视为该患者组的标准治疗方案之一。试验注册:EU试验号:EudraCT: 2021-004981-37。于2021年12月13日注册。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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