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临床试验/NCT00134914
NCT00134914已完成不适用

Effects of Buprenorphine/Naloxone in Treating Opioid Dependent Individuals

National Institute on Drug Abuse (NIDA)2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 1996年8月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
2
主要终点
physiologic measures

研究概览

简要总结

Buprenorphine is a treatment for opioid dependence. Naloxone is given in addition to buprenorphine in order to limit the abuse potential that is commonly associated with buprenorphine. The purpose of this study is to examine the effects of buprenorphine/naloxone when given through different routes and at different doses.

详细描述

Buprenorphine, a mixed agonist-antagonist opioid (or partial agonist), is a safe and effective treatment for opioid dependence. However, there is concern that buprenorphine may be abused due to its high abuse potential. A sublingual buprenorphine/naloxone combination tablet may reduce the risk of abuse associated with buprenorphine alone. The purpose of this study is to characterize the effects of buprenorphine/naloxone in opioid-dependent individuals.

This study will last 10 weeks. Participants will stay in a residential research unit, and will be maintained on oral hydromorphone (10 mg). During twice-weekly experimental sessions, participants will be randomly assigned to receive either sublingual tablets, intramuscular injections, or a placebo. The 15 conditions studied will include: sublingual or intramuscular buprenorphine/naloxone (1/0.25 mg, 2/0.5 mg, 4/1 mg, 8/2 mg, and 16/4 mg), 0.25 mg of intramuscular naloxone (antagonist control), 10 mg of intramuscular hydromorphone (agonist control), sublingual and intramuscular buprenorphine (8 mg), and placebo.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Currently opioid dependent
  • In good health, as determined by a pre-participation medical examination
  • Seeking and eligible for methadone maintenance or detoxification treatment

排除标准

  • Significant medical or psychiatric illness, other than drug dependence

结局指标

主要结局

physiologic measures

时间窗: up to one day

Opioid agonist rating

时间窗: up to one day

opiate withdrawal

时间窗: up to one day

次要结局

未报告次要终点

研究者

申办方类型
Nih

研究点 (2)

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