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临床试验/NCT05300581
NCT05300581已完成不适用

Determining the Feasibility of Outpatient Parenteral Antibiotic Therapy for Persons Who Inject Opioids

Washington University School of Medicine2 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2022年3月16日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
10
试验地点
2
主要终点
Illicit drug use

研究概览

简要总结

Patients with a history of injection drug use are historically excluded from home outpatient parenteral antibiotic therapy programs. Recent small pilot programs have demonstrated that these patients may be safely included in home OPAT programs when they are provided with medications for opioid use disorder such as suboxone or methadone. However nothing is known about the effect of additional social support services including case management and health coach navigation on the feasibility and acceptibility of home OPAT programs for persons who inject drugs. This observational study will provide pilot data on the feasibility of such a program in anticipation of a larger scale trial.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • English speaking males and females
  • 18-100 years of age
  • Being considered for discharge from Barnes-Jewish Hospital on OPAT* (PICC/Midline only) for a serious injection related infection including; endocarditis, osteomyelitis, discitis, septic arthritis, epidural abscess, or S. aureus bacteremia. *Note that outside of this protocol patients with a history of substance use disorder are considered for discharge on OPAT to skilled nursing facilities or other health-care locations such as BJH extended care. Patients being considered for discharge on OPAT to any of these locations are eligible for inclusion.
  • History of injection opioid use within the last 1 year
  • Evaluated by the joint toxicology/psychiatry addiction medicine consult service during the current inpatient admission
  • Started or maintained on medications for opioid use disorder (MOUD) of either methadone, buprenorphine or buprenorphine-naloxone during admission to Barnes-Jewish Hospital
  • Have a scheduled follow-up for continuation of medications for opioid use disorder in place prior to discharge. For patients on methadone this should include a scheduled appointment at a methadone clinic, or for patients on buprenorphine this can include a plan for ongoing buprenorphine/ buprenorphine-naloxone based therapy at the Washington University Infectious Diseases Clinic.
  • Have met with a health coach or a member of the Bridge To Health team during their inpatient hospitalization and agree to ongoing supportive counseling after discharge.
  • Be willing and able to attend in-person clinic visits within 60 days post-discharge at the Washington University Infectious Diseases Clinic.
  • Have a working phone number with active voicemail, running water and electricity.

排除标准

  • Prisoner status
  • Unable to provide own informed consent
  • Current homelessness
  • Other house-hold members reported as having active untreated substance use disorders
  • Unable to attend outpatient appointments. This may include patients who are from rural areas where transportation vouchers may not provide sufficient means of making it to follow-up appointments, or other disability that would preclude transportation (paralysis, broken limbs) where the patient is unable to provide specific details as to how they would arrive at clinic appointments.

结局指标

主要结局

Illicit drug use

时间窗: 6 weeks patient participation

Participants will have urine drug screens performed at clinic follow-up visit while on OPAT.

Completion of parenteral antibiotic therapy

时间窗: 6 weeks patient participation

Participants will be asked to self-report compliance to the recommended IV antibiotic therapy during a telephone survey performed at completion of antibiotic therapy.

次要结局

  • 90-day Overdose(3 month chart review)
  • Sample Size Estimation for Future Study(One year post-enrollment)
  • Survey Completion(3 month chart review)
  • 90-day microbiologic failure(3 month chart review)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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