ISRCTN72781592已完成不适用
Short versus long buprenorphine-naloxone treatment in intravenous buprenorphine withdrawal: a randomised controlled trial
Helsinki Deaconess Institute (Finland)0 个研究点目标入组 120 人开始时间: 2008年3月4日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 120
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Opiate dependence (Diagnostic and Statistical Manual of Mental Disorders - Fourth Edition [DSM IV])
- •2. Current misuse of buprenorphine intravenously (mimimun 3 mg/day) (use confirmed by urinalysis)
- •3. Willingness to participate in withdrawal in the treatment centre and in rehabilitation afterwards
- •4. Aged between 18 and 50
排除标准
- •1. Other than buprenorphine as the primary drug of misuse
- •2. Misuse of other opiates then buprenorphine during the last week (confirmed by urinalysis)
- •3. Opiate maintenance therapy
- •4. Psychotic symptoms at recruitment
- •5. Psychiatric or somatic disease or symptoms that may require hospitalisation at near future
- •6. Salient increase in alanine aminotransferase (ALAT)
- •7. Pregnancy
- •8. Allergy to lofexidine, buprenorphine or naloxone
- •9. Former participation to the same study
- •10. Concurrent participation to other intervention studies
- •11. Native language other than Finnish
研究者
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