The Ohio Valley Node of the Clinical Trials Network

临床试验网络俄亥俄谷节点

基本信息

  • 批准号:
    10652032
  • 负责人:
  • 金额:
    $ 37.9万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2022
  • 资助国家:
    美国
  • 起止时间:
    2022-07-01 至 2023-02-28
  • 项目状态:
    已结题

项目摘要

PUBLIC HEALTH ABSTRACT Medications for Opioid Use Disorder (MOUD), such as methadone, buprenorphine (with or without naloxone), and extended-release naltrexone, have been shown to reduce overdoses and drug use. However, MOUD retention is essential to attaining these outcomes. Unfortunately, only 50% or less of patients remain on MOUD 6 months after initiating treatment, a minimum standard established by the National Quality Forum. One possible approach to improving retention would be using patient characteristics to select the MOUD with which patients are most likely to be successful. This study will utilize VHA data sets to identify patient characteristics associated with improved MOUD retention by MOUD type as well as patient characteristics associated with successful MOUD discontinuation without relapse. We will use a retrospective cohort design using the International Classification of Disease, 9th and 10th edition (ICD-9/10-CM) codes to operationalize OUD since the years of data used for this study cross over the time of ICD-10 implementation (2015). Aim 1 is to identify patient characteristics associated with MOUD retention and opioid overdose death by MOUD type. Our primary outcome for Aim 1 will be a binary measure of retention defined as continuous coverage with the type of MOUD the patient originally initiated for 180 days after the index date without a 28- day gap in treatment. Secondary outcome measures will include (1) a binary measure of retention similar to the primary outcome but over the 365 days after the index date and (2) opioid overdose death in the 365 days after the index date using the VHA Mortality Data Repository. Aim 2 is to quantify the association between probability of relapse after MOUD discontinuation and both length of MOUD therapy and patient characteristics. The outcome for Aim 2 will be discontinuation with vs. without relapse.
公共卫生摘要

项目成果

期刊论文数量(0)
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会议论文数量(0)
专利数量(0)

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T John WINHUSEN其他文献

T John WINHUSEN的其他文献

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{{ truncateString('T John WINHUSEN', 18)}}的其他基金

The Ohio Valley Node of the Clinical Trials Network
临床试验网络俄亥俄谷节点
  • 批准号:
    10621497
  • 财政年份:
    2022
  • 资助金额:
    $ 37.9万
  • 项目类别:
The Ohio Valley Node of the Clinical Trials Network
临床试验网络俄亥俄谷节点
  • 批准号:
    10441828
  • 财政年份:
    2021
  • 资助金额:
    $ 37.9万
  • 项目类别:
The Ohio Valley Node of the Clinical Trials Network
临床试验网络俄亥俄谷节点
  • 批准号:
    10441986
  • 财政年份:
    2021
  • 资助金额:
    $ 37.9万
  • 项目类别:
EMPOWER: Evaluating the ability to reduce Morphine equivalent dose for chronic Pain patients receiving Opioid-therapy through a Web-based E-Health self-management program: a Randomized multi-site Clin
EMPOWER:评估通过基于网络的电子健康自我管理计划减少接受阿片类药物治疗的慢性疼痛患者吗啡当量剂量的能力:随机多站点临床
  • 批准号:
    10174898
  • 财政年份:
    2017
  • 资助金额:
    $ 37.9万
  • 项目类别:
A tailored, peer-delivered intervention to reduce recurring opioid overdoses
量身定制的、同行提供的干预措施,以减少反复出现的阿片类药物过量
  • 批准号:
    9352799
  • 财政年份:
    2016
  • 资助金额:
    $ 37.9万
  • 项目类别:
A tailored, peer-delivered intervention to reduce recurring opioid overdoses
量身定制的、同行提供的干预措施,以减少反复出现的阿片类药物过量
  • 批准号:
    9015947
  • 财政年份:
    2016
  • 资助金额:
    $ 37.9万
  • 项目类别:
Clinical Trials Network, Ohio Valley Node U10DA013732
临床试验网络,俄亥俄谷节点 U10DA013732
  • 批准号:
    8606917
  • 财政年份:
    2000
  • 资助金额:
    $ 37.9万
  • 项目类别:
Clinical Trials Network, Ohio Valley Node U10DA013732
临床试验网络,俄亥俄谷节点 U10DA013732
  • 批准号:
    8656498
  • 财政年份:
    2000
  • 资助金额:
    $ 37.9万
  • 项目类别:
Clinical Trials Network, Ohio Valley Node U10DA013732
临床试验网络,俄亥俄谷节点 U10DA013732
  • 批准号:
    8712426
  • 财政年份:
    2000
  • 资助金额:
    $ 37.9万
  • 项目类别:
Clinical Trials Network, Ohio Valley Node U10DA013732
临床试验网络,俄亥俄谷节点 U10DA013732
  • 批准号:
    8456472
  • 财政年份:
    2000
  • 资助金额:
    $ 37.9万
  • 项目类别:

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阐明丁丙诺啡的高口腔液暴露机制以减少龋齿
  • 批准号:
    10765181
  • 财政年份:
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    10591424
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Providers and Older Pain Patients with Prescription Opioid Dependence: A Qualitative Study to Understand Barriers to Opioid Taper, Cessation, and Transition to Buprenorphine.
具有处方阿片类药物依赖性的提供者和老年疼痛患者:一项定性研究,旨在了解阿片类药物逐渐减少、戒断和过渡到丁丙诺啡的障碍。
  • 批准号:
    10671358
  • 财政年份:
    2023
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Building and Implementing Best Practices for Buprenorphine Initiation in the Setting of Fentanyl Use
在芬太尼使用情况下建立和实施丁丙诺啡起始的最佳实践
  • 批准号:
    10721763
  • 财政年份:
    2023
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长效可生物降解丁丙诺啡储库
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    10757180
  • 财政年份:
    2023
  • 资助金额:
    $ 37.9万
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STANDARD AND HIGH DOSE ED BUPRENORPHINE INDUCTION. 09/15/2023 - 05/31/2026. N01DA-22-2253. TASK ORDER 75N95023F00005 (TO9).
标准和高剂量 ED 丁丙诺啡诱导。
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    10938754
  • 财政年份:
    2023
  • 资助金额:
    $ 37.9万
  • 项目类别:
FY23. TO 11 - CTN-0145: STANDARD VERSUS HIGH DOSE ED-INITIATED BUPRENORPHINE INDUCTION. POP: 8/28/23 - 8/27/24.
23 财年。
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    10938755
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    2023
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    $ 37.9万
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Understanding the Association between Sublingual Buprenorphine and Oral Health Outcomes
了解舌下含服丁丙诺啡与口腔健康结果之间的关联
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    10765299
  • 财政年份:
    2023
  • 资助金额:
    $ 37.9万
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舌下含服与缓释丁丙诺啡对离开监狱环境的个体的有效性比较试验
  • 批准号:
    10718889
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    2023
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    $ 37.9万
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添加丁丙诺啡、认知行为治疗和经颅磁刺激以改善长期阿片类药物治疗慢性疼痛的效果的序贯试验 (ACTION)
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    10717184
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