Buprenorphine as a Treatment for Individuals Dependent on Analgesic Opioids
Dose Reduction Strategies in Oral Opioid Dependence Subsequent to Pain Management: An Exploratory Study
研究概览
详细说明
Many individuals who take opioids for chronic pain abuse the opioid medication. Buprenorphine is an opioid partial agonist that may be effective in treating individuals who abuse opiate pain medication. The purpose of this study is to compare two buprenorphine dosing regimens in order to determine which regimen is more effective in reducing opiate pain medication use and facilitating successful opioid detoxification.
This study will last 27 weeks. Participants will receive a maintenance dose of 8 mg of buprenorphine for 6 weeks, followed by a dose reduction in 2 mg increments over the course of the following 20 weeks. All participants will attend weekly clinical management sessions for the duration of the study.
研究类型
注册
阶段
- 阶段2
联系人和位置
学习地点
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Texas
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Houston、Texas、美国、77030
- University of Texas Health Science Center
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Current opioid analgesic dependence
- History of at least 2 years of oral opiate analgesic use
- Prescribed opioids for chronic pain
- Pain episode of at least 6 months duration within the 5 years prior to study entry
- Available for the duration of the study
- Good general health
Exclusion Criteria:
- Currently using any illicit substance
- Meets criteria for alcohol dependence
- History of heroin use
- History of opiate replacement therapy, including Levo-Alpha Acetyl Methadol (LAAM) or methadone
- Evidence of current maximal primary pain
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
研究衡量的是什么?
主要结果指标
结果测量 |
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治疗保留
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物质使用
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medication compliance
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次要结果测量
结果测量 |
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Behavioral and psychological measures (measured during the dose reduction phase)
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合作者和调查者
调查人员
- 首席研究员:John Grabowski, PhD、University of Texas
研究记录日期
研究主要日期
学习开始
研究完成
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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