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临床试验/NCT03299920
NCT03299920已完成不适用

Opioid Consumption After Knee Arthroscopy With and Without the Use of New Standardized Patient/Family Instructions for Postoperative Analgesic Use

Giorgio Veneziano2 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2017年9月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
17
试验地点
2
主要终点
Number of opioid medication doses taken

研究概览

简要总结

This is a prospective, randomized trial of patients undergoing outpatient knee arthroscopy surgery and receiving a peripheral nerve block. Patients will be randomized to either receive standard discharge teaching or specialized teaching regarding pain control following a nerve block. Patients will be asked to complete a journal for 5 days recording their pain scores, opioid medication usage, and overall satisfaction with pain control at home.

研究设计

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

入排标准

年龄范围
— 至 20 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Patient of age less than 20 years presenting to NCH main campus for knee arthroscopy
  • American Society of Anesthesiology physical status I or II

排除标准

  • Anterior cruciate ligament repair or reconstruction
  • Admission to hospital
  • Inability or refusal to receive femoral nerve blockade
  • Body mass index > 99 percentile
  • Hydrocodone allergy or intolerance
  • Acetaminophen allergy or intolerance
  • Non-steroidal anti-inflammatory allergy or intolerance
  • Pregnancy
  • Interpreter requirement
  • Opioid use within 3 months prior to surgery
  • Previous knee surgery at WSC after Jan. 1, 2017
  • History of opioid abuse or dependence

研究组 & 干预措施

Intervention

Active Comparator

Patients will receive standardized instruction from a study nurse, tailored to understanding pain management after nerve blocks and maximizing utilization of non-opioid analgesics.

干预措施: Standardized instructions (Other)

Control

Other

Patient will receive conventional instructions on postoperative pain management.

干预措施: Conventional instructions (Other)

结局指标

主要结局

Number of opioid medication doses taken

时间窗: Post-op day 5

次要结局

未报告次要终点

研究者

发起方
Giorgio Veneziano
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Giorgio Veneziano

Director, Regional Anesthesia Service

Nationwide Children's Hospital

研究点 (2)

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