跳至主要内容
临床试验/NCT06002724
NCT06002724尚未招募不适用

Feasibility Study of Peripheral Venous Cannulation Pain in Predicting Acute Pain After

RenJi Hospital0 个研究点目标入组 180 人开始时间: 2023年8月30日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
180
主要终点
postoperative resting pain and movement-evoked pain

研究概览

简要总结

The goal of this prospective observational study is to explore the feasibility of preoperative peripheral venous cannulation pain score in predicting acute pain after total knee arthroplasty, including resting pain and movement-evoked pain.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Prospective

入排标准

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

入选标准

  • Patients undergoing the first unilateral total knee arthroplasty surgery under general anesthesia combined with nerve block ;
  • Age : 18 years old ≤ age ≤ 80 years old ;
  • ASA grade I-II ;
  • Informed consent was signed by patients or immediate family members before operation.

排除标准

  • There are known pain abnormalities, mental disorders, cognitive dysfunction ;
  • patients with long-term use of opioids and a history of drug dependence ;
  • patients with alcohol dependence ;
  • the patient refused to use the analgesic pump ;
  • Difficult to understand the VAS score ;
  • body mass index ≥ 40 ;
  • hand nerve abnormalities, hand loss ;
  • plan postoperative ICU patients ;
  • In other cases, the researchers believe that is not suitable for this researcher.

结局指标

主要结局

postoperative resting pain and movement-evoked pain

时间窗: one hour、the first day and the second day after operation

visual analogue scale(VAS) of one hour、the first day and the second day after operation

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

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