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临床试验/NCT04970069
NCT04970069已完成不适用

The Effect of Preoperative Education on Postoperative Opioid Consumption

The Cleveland Clinic2 个研究点 分布在 1 个国家目标入组 1,057 人开始时间: 2021年7月25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
1,057
试验地点
2
主要终点
Opioid Consumption

研究概览

简要总结

The investigators will evaluate the effect of preoperative education on postoperative opioid.

详细描述

The investigators propose a randomized trial to be performed at the Cleveland Clinic. Patients will be assigned to: 1) an educational video focused on postoperative analgesia modalities, opioids, and realistic pain expectations (analgesic education); or, 2) an educational video focused on other aspects of the perioperative experience.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Outcomes Assessor)

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

  • Modified informed consent
  • Adults ≥18 years
  • American Society of Anaesthesiologists physical status 1-4
  • Scheduled for hip arthroplasty, laparoscopy assisted colorectal surgery
  • Personal visit the PACE clinic
  • Anticipated overnight postoperative hospitalization
  • Reasonable English fluency

排除标准

  • Opioid use for more than 30 consecutive days within three preoperative months, at a daily dose of 15 mg or more of morphine or equivalent
  • Regional block or epidural analgesia

结局指标

主要结局

Opioid Consumption

时间窗: 72 hours after surgery

Opioid consumption (morphine milligrams equivalent) during the initial 72 hours after surgery.

次要结局

  • Time-weighted Average Pain Scores(72 hours after surgery, or until discharge, whichever was earlier)
  • Satisfaction With Post Operative Pain Management(3 days after surgery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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