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临床试验/NCT00175357
NCT00175357已完成3 期

North American Opiate Medication Initiative (NAOMI): Multi-Centre, Randomized Controlled Trial of Heroin-Assisted Therapy for Treatment-Refractory Injection Opiate Users

University of British Columbia2 个研究点 分布在 1 个国家目标入组 192 人开始时间: 2005年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
192
试验地点
2
主要终点
Recruitment and retention in the study at 12 months

研究概览

简要总结

The objective of this study is to determine whether the closely supervised provision of injectable, pharmaceutical-grade heroin (in combination with oral methadone) is more effective than methadone therapy alone in recruiting, retaining, and benefiting long-term heroin users who have not been helped by current standard treatment options.

详细描述

This is a two-centre (Vancouver, Montreal) RCT involving a total of 235 volunteers. Eligible participants will be randomized to injectable heroin combined with oral methadone as desired (45%) versus oral methadone alone (45%). A subset of 10% will be randomized to injectable hydromorphone (Dilaudid™). Hydromorphone and heroin will be given in a double-blind fashion; the purpose is to permit validation of reported illicit use of heroin through urine testing in the hydromorphone group. Research visits will be conducted quarterly and will occur independently of treatment clinic visits. Incentives will be used to maintain research follow-up whether or not the subject is retained in treatment. The analysis will be under intent-to-treat. The primary outcomes of interest are 1) recruitment and retention in the study and 2) illicit drug use and criminal behavior (as determined by the Europ-ASI) at 12 months. Secondary outcomes are measures of social function (e.g., social integration and functioning, quality of life) and cost-benefit/effectiveness of the interventions.

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
25 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Opioid Dependence as confirmed by DSM-IV diagnostic criteria
  • 25 years of age or older
  • 5 years or more of opioid use
  • Regular opioid injection use in the past month and in at least 8 months in the past 12 months (self reported; regular use - defined as injecting opioids for at least 4 days or more in a week); 50% or more of the injections during the prior year must have involved heroin).
  • Minimum of one-year residence in site/city location
  • No enrollment in any other opioid substitution (e.g. methadone) program within the prior 6 months - enrollment is defined as having received at least 45 milligrams of prescribed methadone per day on any 30 consecutive days or more in the prior 6 months
  • At least two previous episodes of opiate addiction treatment (methadone maintenance, detoxification, residential care, etc) during which, on at least one occasion, the patient received at least 60 mg of methadone daily for at least 30 days in a 40 day period
  • Willingness and ability to adhere to study protocol and follow-up schedule as determined through the three-week pre-randomization period (see Section C.4)
  • Documentation of fulfillment of the above study criteria (prison records, treatment records, cohort study enrollment, urine sampling)
  • Provide written and informed consent.

排除标准

  • Diagnosis of severe medical or psychiatric conditions that are contra-indicated for heroin treatment
  • Pregnancy upon study entry
  • On parole or with current justice system involvement that is likely to result in an extended period of incarceration (more than 4 months) during the study period (e.g. scheduled trial for an indictable offense, jail, etc)
  • Hydromorphone is a class C teratogen and should not be given to pregnant women. All female subjects upon study entry will be urged to engage only in protected sexual intercourse and will provide consent to undergo monthly pregnancy tests during the course of the study.
  • Serum bilirubin >2.5 x normal
  • Stage II or greater hepatic encephalopathy
  • Chronic respiratory disease resulting in resting respiratory rate >20/minute
  • Bipolar Mood Disorder, Schizophrenia or other psychotic disorder with active psychotic symptoms within the past 6 months
  • Major Depression refractory to medical management or requiring electroconvulsive therapy within the past 12 months.

研究组 & 干预措施

1

Active Comparator

Oral methadone

干预措施: Methadone (Drug)

2

Experimental

Injected diacetylmorphine

干预措施: Diamorphine hydrochloride (Drug)

结局指标

主要结局

Recruitment and retention in the study at 12 months

时间窗: 12 months

Illicit drug use and criminal behavior at 12 months.

时间窗: 12 months

次要结局

  • social integration, functioning, quality of life at 12 and 24 months; and cost-effectiveness at 12 months(24 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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