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临床试验/NCT04927351
NCT04927351进行中(未招募)不适用

Nudges for Opioid Reduction After Major Surgery

University of Washington2 个研究点 分布在 1 个国家目标入组 484 人开始时间: 2021年11月17日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
484
试验地点
2
主要终点
Total Discharge Opioid Burden

研究概览

简要总结

This is a prospective pilot trial to evaluate a new electronic medical record based intervention to improve discharges after surgery. The investigators hypothesize that standard discharge medications after surgery will help to optimize opioid prescribing and potentially decrease healthcare utilization in the first 30 days after surgery.

详细描述

This is a 2-arm parallel randomized trial comparing a new electronic medical record (EMR)-based intervention to usual care after surgery. All patients will receive their usual peri- and intraoperative care. Then, upon discharge, their providers will see the new EMR-based discharge order set (intervention arm) or not (usual care). The investigators hypothesize that standard discharge medication order sets after surgery will help to optimize opioid prescribing and potentially decrease healthcare utilization in the first 30 days after surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
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

  • Adult patients
  • Aged 18 and over
  • Undergo selected general surgical procedures

排除标准

  • Less than 18 years of age

结局指标

主要结局

Total Discharge Opioid Burden

时间窗: Immediately after study intervention

Morphine milligram equivalents in the initial discharge prescription after index surgery

次要结局

  • Additional Opioid Burden within 30 days(Within 30 Days)
  • Proportion of cases with Phone Calls to Surgery Department(Within 30 Days)
  • Proportion of Cases with Hospital Readmissions to a Surgical Service(Within 30 Days)
  • Proportion of Cases with Emergency Room Visits(Within 30 Days)

研究者

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

David Flum

Professor of Surgery

University of Washington

研究点 (2)

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