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临床试验/NCT04885231
NCT04885231已完成不适用

Impact of Counseling and Education on Opioid Consumption After Anterior Cruciate Ligament Reconstruction: A Randomized Controlled Trial

University of Maryland, Baltimore2 个研究点 分布在 1 个国家目标入组 121 人开始时间: 2021年5月12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
121
试验地点
2
主要终点
Postoperative opioid consumption

研究概览

简要总结

Research question: Does an opioid limiting pain management counseling and education program result in decreased opioid consumption and improved pain control compared to traditional pain management programs after anterior cruciate ligament reconstruction (ACLR) surgery?

At many institutions, the current standard of care is to instruct patients to take opioid pain medicine as needed when in severe pain to "stay ahead of the pain." This study is investigating whether modifying the instructions to take opioid pain medications only if in "unbearable pain" will have an effect on 1) reducing opioid consumption and 2) improving pain levels.

Adults who are undergoing an ACLR surgery will be invited to participate in the study and be randomly assigned to one of the two pain management programs. All patients will receive a comprehensive multi-modality pain management treatments and medications. Patients in both groups will receive the same type and amount of all postoperative medications. The only difference will be in the instructions about when to take the opioid medications.

The patients will then be sent an electronic survey twice per day for 2 weeks about their pain levels and number of opioid pills taken.

详细描述

Prescription narcotic pain medications (opioids) were responsible for roughly 17,000 deaths in 2016 in the United States. Orthopedic surgeons were responsible for prescribing the third highest percentage of opioids among physicians in 2009. In recent years, orthopaedic surgeons have used many different types of non-opioid pain medications and methods to reduce patients' opioid after surgery. Opioid dependence can manifest from prescription use, especially in patients who have never used opioids before.

The purpose of this study is to research the effect of different pain management education programs on pain control and opioid use after an anterior cruciate ligament reconstruction (ACLR) surgery. Specifically, does education directed at avoiding opioids unless in "unbearable pain" have any effect on reducing pain levels and opioid consumption in the early postoperative period compared to traditional pain management education?

Patients who agree to participate in this study will be assigned at random to two opioid education programs after ACLR. All patients will be given peri-operative pain management counseling and education. Patients in the experimental group will be instructed to avoid opioids unless in unbearable pain. Patients in the control group will be instructed to take opioid medication as needed for severe pain to "stay ahead" of the pain. Participants in both groups will be prescribed the exact same type and amount of postoperative medications.

Surveys will be sent electronically to patients twice per day for 2 weeks to monitor pain levels and the amount of opioid consumption. Also, patients will be asked to complete demographic and patient-reported outcome questionnaires after surgery. Patients will be involved in the study for 3 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
14 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women aged 14 years and older
  • All patients scheduled to undergo an ACLR with or without concomitant procedures such as arthroscopic cartilage procedures, meniscus repair or meniscectomy, and/or lateral extraarticular tenodesis (anterolateral ligament reconstruction)
  • Willing to participate in a perioperative pain management education and counseling program
  • Willing to track pain levels and opioid consumption through surveys administered via text
  • Willing to receive a perioperative regional nerve block
  • Language skills and cognitive ability required to participate in the study
  • Provision of informed consent

排除标准

  • Revision ACLR
  • Concomitant open cartilage procedures or additional knee ligament repair or reconstruction
  • Concomitant injury that would also influence pain management
  • History of heroin use or opioid abuse requiring treatment
  • If any previous ipsilateral knee surgery except for knee arthroscopy
  • Preoperative Kellgren-Lawrence grade 3 and 4 on weightbearing radiographs
  • An allergy to any of the study medications
  • Previously enrolled in the CARE trial
  • Anticipated problems with the patient returning for follow-up or accurate completion of survey
  • If patient cannot reliably receive texts and use internet to complete surveys

结局指标

主要结局

Postoperative opioid consumption

时间窗: 3 months

The total morphine equivalents (TMEs) consumed by the patient after surgery

次要结局

  • Numeric Pain Scale(Two weeks)
  • Patient Reported Outcomes - Satisfaction with social roles & activities(2 weeks, 6 weeks, 3 months)
  • Patient Reported Outcomes - Physical Function(2 weeks, 6 weeks, 3 months)
  • Patient Reported Outcomes - Pain(2 weeks, 6 weeks, 3 months)
  • Patient Reported Outcomes - Depression(2 weeks, 6 weeks, 3 months)
  • Patient Reported Outcomes - Fatigue(2 weeks, 6 weeks, 3 months)
  • Opioid Prescription Refills(3 months)
  • Patient Satisfaction(2 weeks, 6 weeks, and 3 months)
  • Patient Reported Outcomes - Anxiety(2 weeks, 6 weeks, 3 months)

研究者

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

Jonathan D. Packer, MD

Associate Professor

University of Maryland, Baltimore

研究点 (2)

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