NCT00993746Unknown4 期
Comparison of Onset of Action Between 2% Lidocaine Plus 0.5% Bupivacaine and 0.5% Bupivacaine in Brachial Plexus Anesthesia for Creation of Arteriovenous Fistula in ESRD Patient
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- onset of sensory block
研究概览
简要总结
Will the technique of adding lidocaine to bupivacaine fasten the onset of bupivacaine alone for infraclavicular brachial plexus block in end-stage renal disease (ESRD) patient?
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •ESRD patient for AVF procedure
- •age >17 year
- •BMI 20-35 kg/m2
- •communicable
排除标准
- •BMI > 35 kg/m2 BMI < 20 kg/m2 หรือ BW < 35 kg
- •History of allergy to local anesthetic drugs
- •Pre-operative neurological deficit, Neuromuscular disorder หรือ old CVA
- •Psychiatric disorder
- •Coagulation disorder
- •Uncontrolled seizure
- •Pregnant and lactating women
研究组 & 干预措施
Bupivacaine plus lidocaine
Active Comparator
Group 1: bupivacaine 20 ml plus lidocaine 10 ml
干预措施: Bupivacaine plus lidocaine (Drug)
Bupivacaine alone
Experimental
Group 2: bupivacaine 30 ml
干预措施: Bupivacaine 30 ml (Drug)
结局指标
主要结局
onset of sensory block
时间窗: 24 hour
次要结局
- onset of motor block(24 hour)
研究者
研究点 (1)
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