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临床试验/NCT00684554
NCT00684554已完成2 期

Buprenorphine Maintenance Treatment of Opioid Dependence in Primary Care: A Randomized Clinical Trial of At-Home Versus In-Office Buprenorphine Induction

New York State Psychiatric Institute1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2007年12月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
20
试验地点
1
主要终点
The Primary Outcome Will Include a Comparison of the Proportion of Patients Successfully Inducted One Week After the Initial Primary Care Visit.

研究概览

简要总结

The study will assess the effectiveness of at-home vs. in-office induction for patients entering buprenorphine maintenance at Associates in Internal Medicine (AIM) primary care clinic.

详细描述

Buprenorphine maintenance is an effective treatment for opioid dependence, yet diffusion has been limited. Physician concern about induction is a reported barrier, primarily as buprenorphine may precipitate withdrawal due to its partial opioid agonist activity and high receptor binding affinity. To minimize risk, guidelines recommend in-office assessment and monitoring during induction. As this may not be feasible (e.g., time limitations), many patients are instructed to self-induct at home. While this may facilitate treatment entry, data on at-home induction are limited. The study will assess the effectiveness of at-home vs. in-office induction for patients entering buprenorphine maintenance at Associates in Internal Medicine (AIM) primary care clinic. Currently, patients receive buprenorphine maintenance at AIM as part of standard clinical practice and through an observational study (IRB 5258). Most patients are insured through Medicaid, which covers visit, medication (obtained through prescription from a local pharmacy), lab, and outside psychosocial treatment cost. In this demonstration project, 20 opioid dependent patients will be randomly assigned to at-home or in-office induction, and then monitored for 12 weeks. Ancillary psychosocial treatment will be encouraged but not required. After randomization, AIM clinic and NYSPI research visits will be scheduled weekly for 4 weeks, and then at weeks 8 and 12. The primary outcome will include a comparison of the proportion of patients successfully inducted one week after the initial primary care visit. Secondary outcomes will include: 1) Time to stabilization after buprenorphine initiation assessed by: a) Time until the patient is without withdrawal for two consecutive days, and b) Time until the patient is opioid free for two consecutive weeks; and 3) Retention-in-treatment at 4 and 12 weeks. Other secondary outcomes include patient satisfaction and change in addiction severity. These data will provide important information in buprenorphine initiation in primary care and enable determination of treatment effects size prior to future clinical trials.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • DSM-IV criteria for current opioid dependence with physical dependence and are seeking treatment
  • Recent opioid use
  • Individuals must describe opioids as their primary drug of abuse.
  • 18-65 years of age
  • Able to give informed consent and comply with study procedures
  • Financially able to receive treatment at AIM and obtain medication (e.g., Medicaid)

排除标准

  • DSM-IV opioid dependence without physical dependence
  • Any current Axis I psychiatric disorder(s) as defined by DSM-IV-TR that in the investigator's judgment are unstable or would be disrupted by study participation (e.g., psychosis, active suicidal or homicidal ideation).
  • Individuals who are significant risk for suicide based on their current mental state or history.
  • DSM-IV alcohol or benzodiazepine dependence with physiologic dependence.
  • Pregnancy, lactation. Women must also agree to use a method of contraception with proven efficacy and agree not to become pregnant during the study.
  • Unstable physical disorder that might make participation hazardous.
  • Individuals with a known allergy, sensitivity or adverse reaction to buprenorphine.
  • Past life-threatening idiosyncratic severe opioid withdrawal reaction (e.g., psychosis, seizure)
  • Current buprenorphine maintenance
  • Current long-acting opioid use (e.g., methadone)
  • Inability to read or understand the self-report assessment forms unaided

研究组 & 干预措施

Unobserved-at home

Active Comparator

Buprenorphine Unobserved at home induction

干预措施: Buprenorphine (Drug)

Observed

Active Comparator

Buprenorphine Observed in office induction

干预措施: Buprenorphine (Drug)

结局指标

主要结局

The Primary Outcome Will Include a Comparison of the Proportion of Patients Successfully Inducted One Week After the Initial Primary Care Visit.

时间窗: one week after initial primary care visit

The primary outcome will include a comparison of the proportion of patients successfully inducted one week after the initial primary care visit. Defined as in treatment, on Buprenorphine and withdrawal free.

次要结局

  • Prolonged Withdrawal(a) 2 days)

研究者

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

Frances R Levin

Director of Substance Use Disorder

New York State Psychiatric Institute

研究点 (1)

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