Comparison of effectiveness of ultrasound guided single injection infraclavicular brachial plexus block using bupivacaine alone with bupivacaine combined with dexmedetomidine for pain control in upper limb surgeries.
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- 1. Onset and duration of sensory and motor blockade
研究概览
简要总结
This is a prospective randomised double-blind study comparing the effectiveness of ultrasound guided infraclavicular brachial plexus block using bupivacaine alone with bupivacaine combined with dexmedetomidine in patients undergoing upper limb surgries. It wil be conducted in a total of 50 patients, 25 in each group, in all the hospitals attached to Bangalore Medical College and Research Institute. Primary outcome is to measure the onset and duration of sensory and motor blockade and secondary outcome is duration of analgesia and sedation score including postoperative period.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)(—)
- 性别
- All
入选标准
- •Patients who have given informed and written consent
- •Patients belonging to ASA1 and ASA2 category
- •Patients aged 18-60 years.
排除标准
- •Patients refusing to take part in study
- •Infection at block site
- •Patients with bleeding disorder and abnormal coagulation profile 5.
结局指标
主要结局
1. Onset and duration of sensory and motor blockade
时间窗: Intra operative and Post operative period
2. Duration of analgesia
时间窗: Intra operative and Post operative period
次要结局
- Supplemental opioid requirement and sedation score(Intraoperative and postoperative period)
