CTRI/2025/08/093726尚未招募Phase 3 4
Effect of adding dexmedetomidine to lignocaine with adrenaline in supraclavicular brachial plexus block for approval of subject
goverment multispeciality hospital sector1 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2025年9月8日最近更新:
试验速览
- 阶段
- Phase 3 4
- 状态
- 尚未招募
- 发起方
- 入组人数
- 96
- 试验地点
- 1
- 主要终点
- to determine the duration of analgesia
研究概览
简要总结
this is prospective double blind randomized controlled study, we will be evaluating the effect of adding dexmedetomidine to 1.5 percentage lignocaine adreanaline in ultrasound guided supraclavicular brachial plexus block for upper limb orthopaedic surgeries in terms of duration of analgesia, onset and duration of sensory and motor block, effect on haemodynamic parameters and adverse effects to technique or drugs under study at govt. multispeciality hospital sector 16 A chandigarh
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Double
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •ASA1 and ASA2,2)Age group between 18 to 60 years,3)Patient giving consent for study.
排除标准
- •severe respiratory and cardiovascular disease patients,sensitivity to study drug,known history of bleeding tendency or deranged coagulogram,duration of surgery more than 2 hours,patients with neurodeficit involving brachial plexus,pregnant patients,patients on any alpha2 agonist or antagonist tratment,drug abusers and psychiatric patients.
结局指标
主要结局
to determine the duration of analgesia
时间窗: 12 hours
次要结局
- To determine the onset and duration of sensory and motor block,To determine the effect on haemodynamic parameters,To observe side effects, if any.
研究者
Harish
Government multispeciality hospital
研究点 (1)
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