跳至主要内容
临床试验/NCT07065266
NCT07065266Enrolling By Invitation不适用

The Utility of a Dichotomous Pain Scale in Reducing Postoperative Opioids Consumption in Outpatient ACL Surgery: A Prospective Randomized Controlled Study

Stanford University1 个研究点 分布在 1 个国家目标入组 130 人开始时间: 2020年7月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
130
试验地点
1
主要终点
Amount of opioid medication used post-operatively for 14 days

研究概览

简要总结

The goal of this randomized clinical trial is to compare opioid consumption among patients who receive a binary pain scale compared to those who receive a standard 10-point pain scale after undergoing anterior cruciate ligament (ACL) reconstruction surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
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
否

入选标准

  • •Undergoing ACL reconstruction surgery at Stanford Sports Medicine Redwood City, with autograft or allograft, with or without concomitant meniscal repair.

排除标准

  • •Pregnant women
  • •Surgical history of the operated knee
  • •Known allergy to opioid medications
  • •Received extra-routine pain care (as compared with the average ACL patients at the Sports Medicine division) given by the anesthesiologists, such as the postoperative epidural analgesia or the ultra-sound guided femoral nerve block.

研究组 & 干预措施

10-point pain scale

Active Comparator

participants undergoing ACL reconstructive surgery are asked to use a 10-point NPRS pain scale to describe their pain post-operatively

干预措施: Numerical Pain Rating Scale (NPRS) (Other)

Binary pain questionnaire

Experimental

Participants undergoing ACL reconstructive surgery are asked to describe their pain as tolerable or intolerable post-operatively

干预措施: Binary pain questionnaire (Other)

结局指标

主要结局

Amount of opioid medication used post-operatively for 14 days

时间窗: 14 days post-surgery

次要结局

未报告次要终点

研究者

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

Todd Alamin

Professor of Orthopaedic Surgery

Stanford University

研究点 (1)

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