Comparing Treatments for HIV-Infected Opioid and Alcohol Users in an Integrated Care Effectiveness Study (CHOICES)
2019年3月1日 更新者:P. Todd Korthuis, MD、Oregon Health and Science University
The purpose of this study is to learn how best to treat substance use disorders in an HIV clinic setting.
Specifically, the purpose of this pilot study is to learn if extended-release naltrexone (XR-NTX) would be a feasible and acceptable treatment for HIV-infected individuals with opioid or alcohol use disorders.
研究概览
研究类型
介入性
注册 (实际的)
51
阶段
- 第三阶段
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 100年 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
- Meet Diagnostic and Statistical Manual (DSM-5) criteria for moderate or severe opioid use disorder and/or alcohol use disorder.
- Be willing to be randomized to antagonist-based therapy or treatment as usual (TAU) for treatment of opioid and/or alcohol use disorders.
- Be HIV-infected as defined by history of positive HIV serology or HIV RNA pcr >10,000 copies/mL).
- Be willing to establish ongoing HIV care at community treatment program(CTP) if not already receiving ongoing care.
- Be willing to initiate antiretroviral therapy (ART) if not already prescribed ART, regardless of CD4 count.
- Be at least 18 years old.
- Be able to provide written informed consent and HIPAA (if applicable) for medical record abstraction.
- Be able to communicate in English.
- If female, be willing to take measures to avoid becoming pregnant.
Exclusion Criteria:
Individuals will be excluded from pilot study participation if they:
- Have a serious medical, psychiatric or substance use disorder that, in the opinion of the study physician, would make study participation hazardous to the participant, compromise study findings, or prevent the participant from completing the study.
Examples include:
Disabling or terminal medical illness (e.g., active opportunistic infection, uncompensated heart failure, cirrhosis or end-stage liver disease, acute hepatitis and moderate to severe renal impairment) as assessed by medical history, review of systems, physical exam and/or laboratory assessments;
- Severe, untreated or inadequately treated mental health disorder (e.g., active psychosis, uncontrolled manic-depressive illness) as assessed by history and/or clinical interview;
- Current severe benzodiazepine or other depressant or sedative hypnotic use requiring medical detoxification;
- Suicidal or homicidal ideation requiring immediate attention.
- Have aspartate aminotransferase (AST) or alanine aminotransferase (ALT) liver enzymes greater than 5 times upper limit of normal on screening phlebotomy. Results from tests conducted within the past 30 days which are abstracted from medical record information are acceptable.
- Have international normalized ratio (INR) > 1.5 or platelet count <100k. Results from tests conducted within the past 30 days which are abstracted from medical record information are acceptable.
- Have known allergy or sensitivity to naloxone, naltrexone, polylactide-co-glycolide, carboxymethylcellulose, or other components of the Vivitrol® diluents.
- Anticipate undergoing surgery during study participation.
- Have chronic pain requiring ongoing pain management with opioid analgesics.
- Pending legal action or other reasons that might prevent an individual from completing the study.
- Currently pregnant or breastfeeding.
- Body habitus that, in the judgment of the study physician, precludes safe intramuscular injection of XR-NTX, (e.g. excess fat tissue over the buttocks).
- Received methadone or buprenorphine maintenance therapy for treatment of opioid dependence in the 4 weeks prior to screening.
- Have taken an investigational drug in another study within 30 days of study consent.
- Have ECG findings that, in the opinion of the study medical clinician would preclude safe participation in the study. Results from ECGs conducted within the past 30 days which are abstracted from medical record information are acceptable.
- Have had treatment with XR-NTX for opioid or alcohol dependence in the 3 months prior to screening.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
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有源比较器:Treatment as Usual
The current standard of care for treatment of opioid use disorders in HIV clinics is opioid agonist therapy.
HIV-infected patients with alcohol use disorders are typically referred for residential, outpatient, and self-help groups.
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实验性的:Extended Release Naltrexone
Extended release naltrexone (XR-NTX), delivered by monthly injection.
Dose: 380 mg.
Frequency: One injection per month, for four months.
Duration: 30 days.
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其他名称:
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of Participants With Successful Initiation of Treatment Within 4 Weeks of Randomization
大体时间:4 weeks
|
Successful induction onto XR-NTX or initiation of treatment as usual within 4 weeks of randomization.
|
4 weeks
|
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Number of Participants Successfully Retained on Pharmacotherapy Treatment at 16 Weeks
大体时间:16 weeks
|
Number of participants who received the maximum possible expected doses of XR-NTX, or the full course of recommended pharmacotherapy treatment for treatment as usual (TAU) arm.
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16 weeks
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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HIV Viral Suppression at 16 Weeks
大体时间:16 weeks
|
Plasma HIV viral load of < 200 copies/mL compared with screening
|
16 weeks
|
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Mean Days of Opioid Use in Past 30 Days
大体时间:Baseline and 16 weeks
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Change in 30 day opioid use by Addiction Severity Index (ASI)-lite self-report and Time-Line Follow Back in the final 30 days of the 16 week trial compared to screening.
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Baseline and 16 weeks
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HIV Care Engagement
大体时间:Baseline and 16 weeks
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Change in the proportion of participants prescribed antiretroviral therapy (ART) within 16 weeks following randomization, compared to baseline.
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Baseline and 16 weeks
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Participant Safety: Change in Liver Enzymes Between Baseline and Week 16
大体时间:Baseline and 16 weeks
|
Change in liver enzymes between screening and Week 16.
AST = Aspartate transaminase ALT = Alanine transaminase
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Baseline and 16 weeks
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Number of Participants With Urine Drug Screen (UDS) Positive for Opioids
大体时间:Baseline and 16 weeks
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Baseline and 16 weeks
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Mean Days of Alcohol Use in Past 30 Days
大体时间:Baseline and 16 weeks
|
Change in 30 day alcohol use by Addiction Severity Index (ASI)-lite self-report and Time-Line Follow Back in the final 30 days of the 16 week trial compared to screening.
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Baseline and 16 weeks
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Number of Participants With Urine Ethyl Glucuronide (EtG) Positive for Alcohol
大体时间:Baseline and 16 weeks
|
Baseline and 16 weeks
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Participant Safety: Any Fatal or Non-fatal Overdose Between Baseline and Week 16
大体时间:16 weeks
|
16 weeks
|
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Participant Safety: Precipitated Withdrawal
大体时间:16 weeks
|
Proportion of participants assigned to XR-NTX who develop precipitated opioid withdrawal.
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16 weeks
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2014年6月1日
初级完成 (实际的)
2015年3月1日
研究完成 (实际的)
2015年3月1日
研究注册日期
首次提交
2013年7月23日
首先提交符合 QC 标准的
2013年7月23日
首次发布 (估计)
2013年7月25日
研究记录更新
最后更新发布 (实际的)
2019年3月19日
上次提交的符合 QC 标准的更新
2019年3月1日
最后验证
2019年3月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.