A Randomized Controlled Trial : Comparison of 4% Articaine Versus 0.5% Bupivacaine for Ambulatory Orthopaedic Surgery Under Supraclavicular Block
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Duration of analgesia
研究概览
简要总结
Effect of 2%Articaine versus 5%bupivacaine in pt undergoing short duration surgery in upper limb
详细描述
The investigator aim to compare Articaine 2% versus bupivacaine 0.5% in patient undergoing upper limb procedure under ultrasound guided supraclavicular block as regard onset and duration of sensory and motor block
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •upper limb surgery
- •ganglion removal
- •Carapal tunnel
排除标准
- •Coagulopathy.
- •infection at site of injection.
- •patient refusal.
- •hypersensitivity.
研究组 & 干预措施
Articaine group
Patients in this group are assigned to recieve 30 ml of Articaine 2%
干预措施: Articaine (Drug)
Bupivacaine
Patients in this group are assigned to recieve 30 ml of bupivacaine 0.5%
干预措施: Bupivacaine (Drug)
结局指标
主要结局
Duration of analgesia
时间窗: Measured in minutes over 24 hours
Measured by numerical analog scale where 0 no pain and 10 means worst pain
Duration of sensory block
时间窗: Measured in minutes over 24 hours
By pinprick test from 0 to 2 where 0 no sensory block and 2 complete anesthesia
Durations of motor block
时间窗: Measured in minutes over 24 hours
By Bromage scale from 1 to 4 where 1 no motor power and 4 full motor power
次要结局
- Analgesia(24 hours)
研究者
simon Halim Armanious
Principal investigator
Ain Shams University