Suboxone: (Buprenorphine/Naloxone) Comparison of Two Taper Schedules

University of California, Los Angeles21 个研究点分布在 1 个国家目标入组 516 人开始时间: 2003年6月1日最近更新: 2017年1月12日

适应症

试验速览

阶段: 3 期
状态: 已完成
发起方: University of California, Los Angeles
入组人数: 516
试验地点: 21
主要终点: Opiate abstinence

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The purpose of this protocol is to to compare the clinical utility of two dosage tapering regimens in Buprenorphine/Naloxone stabilized subjects for opiate detoxification.

研究设计

研究类型: Interventional
主要目的: Treatment

入排标准

年龄范围: 15 Years 至 99 Years（Child, Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Females are not pregnant or lactating
•Subjects meet DSM-IV criteria for opiate dependence, are medically and psychiatrically stable, and do not have a current history of benzodiazepine dependence abuse, dependence, or treatment

排除标准

未提供

结局指标

主要结局

Opiate abstinence

次要结局

未报告次要终点

研究者

发起方

University of California, Los Angeles

申办方类型

Other

研究点 (21)

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