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临床试验/NCT04387097
NCT04387097已完成不适用

Postoperative Drip-infusion of Remifentanil for Preventing Remifentanil-induced Hyperalgesia- a Retrospective Observative Study

Tri-Service General Hospital1 个研究点 分布在 1 个国家目标入组 559 人开始时间: 2018年5月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
559
试验地点
1
主要终点
comparison of the numeric rating scale (NRS) between 2 groups

研究概览

简要总结

The development of remifentanil-induced hyperalgesia (RIH) is an unpleasant experience for surgical patients. An alternative management, gradual withdrawal of remifentanil was effective in prevention of RIH. The investigators designed a simple modality to assess if under withdrawal of remifentanil and further drip-infusion of remifentanil immediately after extubation affected postoperative pain score, the requirement of rescue analgesics, and adverse effects.

详细描述

In clinical practice, the gradual withdrawal of remifentanil during surgery is unsatisfied. Thus, the investigators conducted a simple modality in a single center retrospective cohort study to assess how under baseline gradual withdrawal of remifentanil and further drip infusion of remifentanil immediately after extubation affected postoperative pain score and use of analgesics.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • American Society of Anesthesiologists (ASA) score of I-III patients receiving total intravenous anesthesia

排除标准

  • The use of inhalation agents or propofol combined with inhalation anesthesia
  • Pregnancy
  • Previous substance abuse
  • Known allergies to opioids, propofol or any drugs used in the study
  • History of neuropsychiatric disorder
  • Age < 20 years or > 80 years

研究组 & 干预措施

gradual withdrawal following by drip-infusion of remifentanil

In the end of the surgery, gradual withdrawal of remifentanil was prescribed until the endotracheal tube was extubated. Following by drip-infusion of remifentanil for 30 minutes was administered immediately after tracheal extubation.

干预措施: remifentanil (Drug)

结局指标

主要结局

comparison of the numeric rating scale (NRS) between 2 groups

时间窗: one hour

NRS scores is labeled from zero to ten, with zero being an example of someone with no pain and ten being the worst pain possible.

requirement for rescue analgesics

时间窗: one hour

postoperative requirement for rescue analgesics

次要结局

  • type of surgery(three hours)
  • surgical site(three hours)

研究者

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

Yi-hsuan Huang

Principal Investigator

Tri-Service General Hospital

研究点 (1)

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Drip-infusion of Remifentanil for RIH | 临床试验