跳至主要内容
临床试验/NCT00879996
NCT00879996已完成4 期

A Randomized Controlled Trial Comparing Buprenorphine and Methadone for Opioid Dependent Chronic Pain Patients

State University of New York at Buffalo2 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2009年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
54
试验地点
2
主要终点
Number of Participants Retained in Treatment

研究概览

简要总结

The purpose of this study is to determine if buprenorphine or methadone is better for the treatment of chronic pain among patients who have become addicted to prescription narcotics.

详细描述

The purpose of this randomized clinical trial is to compare methadone with buprenorphine for the treatment of chronic pain among patients who have developed a physical dependence on prescription opiate analgesics that is associated with psychosocial dysfunction (i.e., addiction).

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
None

入排标准

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

入选标准

  • chronic back pain
  • opioid addiction
  • not successful with abstinence
  • at least 18 years old
  • able to understand spoken English
  • live in Western New York State (Erie or Niagara county)
  • have health insurance or ability to pay for health care
  • no methadone or buprenorphine treatment within past year
  • not member of a vulnerable population (e.g., pregnancy, prisoner)

排除标准

  • homelessness
  • unable to give consent (e.g., dementia, psychosis)
  • serious heart or lung disease
  • taking a medication that could interact with methadone or buprenorphine
  • pregnancy

研究组 & 干预措施

1

Active Comparator

Methadone 10-60 mg per day in 2-4 divided doses for 6 months

干预措施: Methadone (Drug)

2

Experimental

Buprenorphine 4-16 mg per day in 2-4 divided doses for 6 months (using tablets of buprenorphine/naloxone:4/1 mg)

干预措施: Buprenorphine/naloxone (Drug)

结局指标

主要结局

Number of Participants Retained in Treatment

时间窗: 6 months

This outcome assesses the number of participants who completed the treatment after 6 months.

次要结局

  • Numerical Rating Score for Pain(6 months)
  • Numerical Rating Score for Functioning(6 months)
  • Self-reported Illicit Opioid Use(6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Richard Blondell

MD

State University of New York at Buffalo

研究点 (2)

Loading locations...

相似试验