Evaluating Suvorexant for Sleep Disturbance in Opioid Use Disorder

评估 Suvorexant 对阿片类药物使用障碍患者睡眠障碍的影响

基本信息

  • 批准号:
    9790420
  • 负责人:
  • 金额:
    $ 113.91万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2019
  • 资助国家:
    美国
  • 起止时间:
    2019-04-01 至 2021-03-31
  • 项目状态:
    已结题

项目摘要

More than 500,000 people sought opioid use disorder (OUD) treatment from state-certified addiction treatment facilities in 2016, and the most frequently accessed form of treatment was supervised opioid withdrawal (also known as detoxification). There has been surprisingly little empirical investigation into mechanisms underlying individual opioid withdrawal symptoms and corresponding best practices for their management. A recent FDA public meeting that included patients with OUD identified sleep disturbance as a primary contributor to OUD treatment failure. The scientific premise of this phased UG3/UH3 proposal is that suvorexant (SUVO; Belsomra®) will improve total sleep time in patients undergoing routine supervised withdrawal from opioids (UG3), and that SUVO will outperform a medication that is commonly administered for that indication (trazodone; UH3). SUVO is a dual orexin receptor antagonist that is FDA-approved for insomnia and is well- suited for this study because it has low abuse potential, improves sleep continuity and architecture with a single dose, has an extremely safe and mild side effect profile, has clear interactions with the opioid system, and has not yet been evaluated in OUD patients. Our interdisciplinary study team includes several experts in OUD and sleep and our proposal provides preliminary evidence of sleep impairment during OUD withdrawal. The UG3 (N=36) and UH3 (N=60) studies will use identical methods and will vary only in the medications examined. OUD patients will be admitted to a residential research unit for 11 days, and will be stabilized on buprenorphine for 3 days before undergoing a 4-day routine taper and a 4-day post-taper period. Study medication will be double-blinded and will begin on Taper day 1. Primary outcomes will be objective sleep measures (unobtrusive EEG via the Sleep ProfilerTM and wrist-worn actigraph) and abuse liability. Secondary measures will include objective, biological, and self-report measures of opioid withdrawal severity, treatment retention, craving, and stress. The UG3 phase will be a dose-finding study of SUVO (10mg, 20mg) compared to placebo. The go-no go decision (i.e. milestone) for UH3 transition will be if either SUVO dose produces a mean increase in total sleep time of at least 10 minutes relative to placebo during the taper. The UH3 phase will be a comparative efficacy trial of trazodone (100mg) vs. the SUVO dose identified in the UG3, to evaluate whether SUVO improves sleep compared to a regularly used sleep aid during opioid withdrawal. After the UH3, results will be collapsed across both studies to examine sleep and withdrawal associations more generally, and men and women will be equally enrolled in both studies to enable sex subgroup comparisons. We hypothesize SUVO will improve total sleep time during withdrawal, will not show evidence of abuse liability, and will be more efficacious than trazodone. Results will advance the treatment of OUD, the understanding of sleep and opioids, and the use of SUVO in clinical populations. These data may also support more prospective evaluations into the use of SUVO as an OUD craving medication.
超过50万人从国家认证的成瘾治疗中寻求阿片类药物使用障碍(OUD)治疗

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Kelly E Dunn其他文献

The IMPOWR Network Divided or Single Exposure Study (DOSE) Protocol: A Randomized Controlled Comparison of Once Versus Split Dosing of Methadone for the Treatment of Comorbid Chronic Pain and Opioid Use Disorder.
IMPOWR 网络分次或单次暴露研究 (DOSE) 方案:一次与分次给药美沙酮治疗共病慢性疼痛和阿片类药物使用障碍的随机对照比较。
  • DOI:
  • 发表时间:
    2024
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Greer McKendrick;Will Davis;Michael Sklar;Nicole Brown;Emma Pattillo;Patrick H. Finan;Denis Antoine;Vickie Walters;Kelly E Dunn
  • 通讯作者:
    Kelly E Dunn
The Public Health Challenge of Δ8-THC and Derived Psychoactive Cannabis Products.
Δ8-THC 和衍生的精神活性大麻产品的公共卫生挑战。

Kelly E Dunn的其他文献

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{{ truncateString('Kelly E Dunn', 18)}}的其他基金

Discovery to Commercialization Program for Substance Abuse Prevention and Treatment (D2C: SAPT)
药物滥用预防和治疗发现到商业化计划(D2C:SAPT)
  • 批准号:
    10524311
  • 财政年份:
    2022
  • 资助金额:
    $ 113.91万
  • 项目类别:
Randomized Clinical Trial Intervention to Treat Chronic Pain Among Persons Maintained on Methadone for Opioid Use Disorder
随机临床试验干预治疗因阿片类药物使用障碍而维持美沙酮治疗的慢性疼痛
  • 批准号:
    10624868
  • 财政年份:
    2022
  • 资助金额:
    $ 113.91万
  • 项目类别:
Discovery to Commercialization Program for Substance Abuse Prevention and Treatment (D2C: SAPT)
药物滥用预防和治疗发现到商业化计划(D2C:SAPT)
  • 批准号:
    10665788
  • 财政年份:
    2022
  • 资助金额:
    $ 113.91万
  • 项目类别:
Randomized Clinical Trial Intervention to Treat Chronic Pain Among Persons Maintained on Methadone for Opioid Use Disorder
随机临床试验干预治疗因阿片类药物使用障碍而维持美沙酮治疗的慢性疼痛
  • 批准号:
    10458799
  • 财政年份:
    2022
  • 资助金额:
    $ 113.91万
  • 项目类别:
Assessing a Clinically-meaningful Opioid Withdrawal Phenotype
评估具有临床意义的阿片类药物戒断表型
  • 批准号:
    10580802
  • 财政年份:
    2021
  • 资助金额:
    $ 113.91万
  • 项目类别:
Assessing a Clinically-meaningful Opioid Withdrawal Phenotype
评估具有临床意义的阿片类药物戒断表型
  • 批准号:
    10401839
  • 财政年份:
    2021
  • 资助金额:
    $ 113.91万
  • 项目类别:
Evaluating Suvorexant for Sleep Disturbance in Opioid Use Disorder
评估 Suvorexant 对阿片类药物使用障碍患者睡眠障碍的影响
  • 批准号:
    9899225
  • 财政年份:
    2019
  • 资助金额:
    $ 113.91万
  • 项目类别:
Evaluating Suvorexant for Sleep Disturbance in Opioid Use Disorder
评估 Suvorexant 对阿片类药物使用障碍患者睡眠障碍的影响
  • 批准号:
    10454583
  • 财政年份:
    2019
  • 资助金额:
    $ 113.91万
  • 项目类别:
A118G SNP and OPRM1 Gene Opioid-Mediated Effects in Humans
A118G SNP 和 OPRM1 基因阿片类药物介导的人类作用
  • 批准号:
    8925834
  • 财政年份:
    2014
  • 资助金额:
    $ 113.91万
  • 项目类别:
A118G SNP and OPRM1 Gene Opioid-Mediated Effects in Humans
A118G SNP 和 OPRM1 基因阿片类药物介导的人类作用
  • 批准号:
    8594898
  • 财政年份:
    2014
  • 资助金额:
    $ 113.91万
  • 项目类别:
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