跳至主要内容
临床试验/jRCTs062240013
jRCTs062240013进行中(未招募)不适用

High-frequency variability index-guided remifentanil versus standard care in lower extremity arthroplasty during general anesthesia: A randomized controlled trial

未提供0 个研究点目标入组 50 人开始时间: 2024年6月25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
50
主要终点
-

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized Controlled Trial
干预模型
Parallel Assignment
主要目的
Other
盲法
Single Blind

入排标准

年龄范围
18age old over 至 No limit(—)
性别
All

入选标准

  • 1.Patients scheduled to undergo unilateral knee or hip replacement under general anesthesia
  • 2.Patients who are 18 years of age or older at the time of consent (regardless of gender)
  • 3.Patients scheduled to enter the PACU after surgery
  • 4.Patients who have received sufficient explanation and informed written consent of their own free will to participate in this study.

排除标准

  • Patients with a history of hypersensitivity to medications to be used during anesthesia
  • Patients with a preoperative ASA-PS (American Society of Anesthesiologists Physical Status) of 3 or higher
  • Patients who have undergone surgery under general anesthesia at least 1 week before the scheduled surgery
  • Patients who have been using narcotic analgesics and antiarrhythmic drugs regularly before the surgery
  • Patients with a history of atrial fibrillation
  • Patients with a pacemaker
  • Patients who are undergoing surgery other than TKAt or THA at the same time.
  • Patients who do not understand Japanese and cannot perform NRS evaluation.
  • Other patients judged inappropriate as research subjects by the principal investigator and subinvestigators.

结局指标

主要结局

-

Amount of remifentanil used during surgery

次要结局

  • NRS(from the time of admission to the PACU to the day after surgery)
  • Use of supplemental analgesia(from the time of admission to the PACU to the day after surgery)
  • Complications
  • Vital signs(during surgery)
  • HFVI values

研究者

发起方
未提供

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