NCT06002724尚未招募不适用
Feasibility Study of Peripheral Venous Cannulation Pain in Predicting Acute Pain After
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
- 是
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
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