A Comparison of Pain Severity on Injection of MCT/LCT Propofol Between Lidocaine 20 mg, 40 mg, and Without Lidocaine.
研究概览
详细说明
Background: Intravenous injection of propofol produces pain. Many factors are involved and various techniques have been tried to minimize the propofol-induce pain with variable results.
Objective: To compare the severity of pain on injection of MCT/LCT propofol with lidocaine 20 mg, 40 mg, and without lidocaine.
Design: Randomize controlled trial. Method: Two hundred and ten ASA class I - III patients undergoing elective surgery were blinded and equally allocated into 3 groups. Patients in group N, L1, and L2 received MCT/LCT propofol 10 ml mixed with 0.9% NaCl 2 ml, 1% lidocaine 2 ml, and 2% lidocaine 2 ml respectively. Pain at time of propofol injection was assessed by blinded anesthesiologist on a four point scale ; 0 = no pain, 1 = mild pain, 2 = moderate pain, and 3 = severe pain. Results: Patient's demographic data of each group were similar. There were significant differences in the incidence of propofol injection without pain among groups (p<0.001). The numbers of patients who had moderate and severe pain in groups L1 and L2 were significantly less than those in group N (p<0.001). The mean blood pressure and heart rate were not significant differences in among groups. Conclusion : The amount of 20 mg, and 40 mg lidocaine to MCT/LCT propofol in our study is equally effective in decreasing pain and more effective than MCT/LCT propofol alone group significantly. They were no significant differences in hemodynamics change in among groups.
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
Songkhla
-
Hatyai、Songkhla、泰国、90110
- Songklanagarind Hospital
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- ASA class I - III patients
- undergoing elective surgery
- age 18-75 years
Exclusion Criteria:
- allergy to propofol and lidocaine
- abnormal liver and renal functions
- has psychological problem or drug abuse
- has recieved analgesic drug 2 weeks prior to surgery
- risk of aspiration
学习计划
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:三倍
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:lidocaine 20 mg
intravenous lidocaine
|
dosage 20 mg and 40 mg
|
|
实验性的:lidocaine 40 mg
intravenous lidocaine 40 mg
|
dosage 20 mg and 40 mg
|
|
安慰剂比较:normal saline
2 ml
|
dosage 20 mg and 40 mg
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
pain on injection
大体时间:30 minutes
|
4 points score for pain:o=no pain,1=mild pain,2=moderate pain,3=severe pain after propofol injection
|
30 minutes
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
hemodynamic change
大体时间:30 minutes
|
blood pressure and heart rate after propofol injection
|
30 minutes
|
合作者和调查者
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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