Dexmedetomidine versus dexamethasone as adjuvants to 0.5% Levobupivacaine in ultrasound guided supraclavicular brachial plexus block
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 90
- 试验地点
- 1
- 主要终点
- Each participant in the study will be assessed for following primary outcome parameters are as follows:-
研究概览
简要总结
Different adjuvants are used with levobupivacaine for supraclavicular block which decrease the onset time and enhanced the duration of the sensory ,motor blockade and duration of analgesia with minimal systemic side effects.
As limited literature is available for comparison .so this study compares levobupivacaine and combination of levobupivacaine with dexmedetomidine versus dexamethasone as adjuvants in ultrasound guided supraclavicular brachial plexus block.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant, Investigator and Outcome Assessor 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
- •Upper limb surgeries Written and informed consent ASA Physical status 1 and 2.
排除标准
- •Bleeding diathesis Hypersensitivity to local anaesthesia Neuromuscular disorders and significant systemic disease.
结局指标
主要结局
Each participant in the study will be assessed for following primary outcome parameters are as follows:-
时间窗: Onset of sensory and motor block will be assessed every 2minute till 30 minute. | Time period from the end of LA administration to complete resolution of sensory block and return to complete motor function will be taken duration of sensory and motor block.
To compare the onset of sensory and motor block
时间窗: Onset of sensory and motor block will be assessed every 2minute till 30 minute. | Time period from the end of LA administration to complete resolution of sensory block and return to complete motor function will be taken duration of sensory and motor block.
To compare the duration of sensory and motor block.
时间窗: Onset of sensory and motor block will be assessed every 2minute till 30 minute. | Time period from the end of LA administration to complete resolution of sensory block and return to complete motor function will be taken duration of sensory and motor block.
次要结局
- Each participant in the study will be assessed for following secondary outcome parameters are as:-(To compare the duration of first rescue analgesia.)
研究者
Dr Niketa Jain
Teerthanker Mahaveer medical college and research centre ,Moradabad