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临床试验/NCT03150173
NCT03150173已完成2 期

Buprenorphine Treatment at Syringe Exchanges to Reduce Opioid Misuse and HIV Risk

Montefiore Medical Center3 个研究点 分布在 1 个国家目标入组 97 人开始时间: 2019年1月2日最近更新:
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
97
试验地点
3
主要终点
Buprenorphine Engagement

研究概览

简要总结

This trial will recruit syringe exchange participants with opioid use disorder in New York City and test whether starting buprenorphine treatment at the syringe exchange program is more effective than referral to a community health center for buprenorphine treatment.

详细描述

In a 24 week randomized controlled trial based in a large urban area with high rates of opioid use disorder (OUD) and HIV, 250 out-of-treatment opioid users who utilize syringe exchanges will be recruited and randomize to receive an onsite treatment intervention (O-BMT) or enhanced referral to buprenorphine treatment. Over 2 weeks, participants in the O-BMT arm will see a buprenorphine provider twice, receive weekly blister packs of medication, and then their care will be transferred to a community health center for maintenance buprenorphine treatment. In the control arm, participants will receive enhanced referral to the community health center for maintenance buprenorphine treatment. Data collection will include urine drug tests, questionnaires, and medical and pharmacy record review. Key outcomes will include engagement in buprenorphine treatment, treatment outcomes, and programmatic costs. Buprenorphine diversion will be assessed by using electronic monitors that estimate medication adherence, testing urine samples for buprenorphine, and through sequential surveys regarding buying or selling illicit buprenorphine.

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

  • age ≥ 18 years
  • opioid use disorder
  • interest in buprenorphine treatment
  • motivation for opioid use disorder treatment
  • willingness to accept community health center referral
  • syringe exchange participant

排除标准

  • receiving opioid agonist treatment in the past 30 days (confirmed by New York Prescription Drug Monitoring Program);
  • inability to provide informed consent
  • unstable mental illness (e.g., suicidality, psychosis, etc.)
  • severe alcohol use disorder or benzodiazepine use disorder by the Diagnostic and Statistical Manual of Mental disorders, Fifth Edition (DSM-5) criteria
  • hypersensitivity to buprenorphine or naloxone.
  • pregnancy (confirmed via urine testing)

研究组 & 干预措施

O-BMT (onsite treatment)

Experimental

Over 2 weeks at the syringe-exchange program, participants in the O-BMT arm will see a buprenorphine provider twice, receive weekly blister packs of medication, and then their care will be transferred to a community health center for maintenance buprenorphine treatment

干预措施: Onsite treatment (Behavioral)

O-BMT (onsite treatment)

Experimental

Over 2 weeks at the syringe-exchange program, participants in the O-BMT arm will see a buprenorphine provider twice, receive weekly blister packs of medication, and then their care will be transferred to a community health center for maintenance buprenorphine treatment

干预措施: Buprenorphine (Drug)

Enhanced Referral

Active Comparator

In the control arm, participants will receive enhanced referral to a community health center for maintenance buprenorphine treatment

干预措施: Enhanced referral (Behavioral)

Enhanced Referral

Active Comparator

In the control arm, participants will receive enhanced referral to a community health center for maintenance buprenorphine treatment

干预措施: Buprenorphine (Drug)

结局指标

主要结局

Buprenorphine Engagement

时间窗: 30 days after randomization

Buprenorphine engagement was defined as the number of participants having an active buprenorphine prescription at 30 days after randomization. Responses were tallied using a dichotomous (i.e., Yes/No) measure. Data are summarized by study arm.

次要结局

  • Treatment Retention(6 months)
  • Incremental Cost-effectiveness Ratio (ICER)(6 months)
  • Quality-adjusted Life-years (QALYs) Gained(6 months)
  • Mean Difference in Total Costs(6 months)
  • Time to First Buprenorphine Prescription(1 month)
  • HIV Risk Behaviors(6 months)
  • Buprenorphine Diversion(6 months)
  • Total Time Prescribed Buprenorphine(6 months)
  • Number/Percentage of Participants Who Received Any Buprenorphine Prescription(6 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (3)

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