CTRI/2017/06/008817尚未招募未知
Effect of Concurrent Administration of Intravenous Naloxone on Opioid Agonist Effects of Intravenous Buprenorphine: A Double-blind, Within-subject, Randomized, Cross-over Study among Opioid Dependent Subjects
ational Drug Dependence Treatment Centre AIIMS0 个研究点目标入组 12 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 12
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
入选标准
- •1. Diagnosed patients of opioid dependence (as per ICD 10 criteria)
- •2. History of injecting drug use ever in life
- •3. Should be on sublingual buprenorphine or buprenorphine-naloxone combination tablets from NDDTC for at least 3 months
- •4. Maintained on sublingual buprenorphine or buprenorphine-naloxone combination dose of 8 to 18 mg per day
- •5. Received sublingual buprenorphine or buprenorphine-naloxone combination tablets on at least 75% of the scheduled occasions in previous three months.
- •6. Willing to provide informed consent
- •7. Able to read and write
排除标准
- •1. Current dependence on substances other than opioids (except nicotine)
- •2. Use of any other psychoactive substance (except nicotine and prescribed psychotropic medications) within the last 72 hours
- •3. Any current general medical illnesses or neurological disorder, psychiatric illnesses or disability hampering communication / informed consent process.
研究者
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