跳至主要内容
临床试验/NCT00000206
NCT00000206已完成2 期

Clinical Rescue Protocol

University of California, Los Angeles2 个研究点 分布在 1 个国家开始时间: 1991年4月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
试验地点
2
主要终点
Retention

研究概览

简要总结

The purpose of this study is to detect increasing medication dose results in heroin cessation for patients still using, to determine if decreasing medication dose in patients unable to tolerate medication dose increases retention, and to determine if blood levels of methadone or buprenorphine correlate with clinical response.

研究设计

研究类型
Interventional
主要目的
Treatment
盲法
Double

入排标准

年龄范围
21 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • M/F ages 21-
  • Opiate dependence according to DSM-IV criteria. Self-reported use within the last 30 days. Agreeable to conditions of study and signed informed consent.

排除标准

  • Psychiatric disorder that requires medication therapy. History of seizures. Pregnant and/or nursing women. Dependence on ETOH or benzodiazepines or other sedative-hynotics. Acute hepatitis. Other medical conditions that deem participation to be unsafe.

结局指标

主要结局

Retention

Opiate use

Opiate craving

Adverse events

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (2)

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