CTRI/2018/07/014690尚未招募不适用
An Evaluation of the effect of intravenous dexmedetomidine and clonidine on the characteristics of subarachnoid block (SAB) by bupivacaine in Trans-ABdominal Hysterectomy (TAH).
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- To Evaluate of the effect of Intravenous Dexmedetomidine and Clonidine on the characteristics of Subarachnoid block by Bupivacaine in Trans-Abdominal Hysterectomy
研究概览
简要总结
This is a Randomized, prospective double blind placebo control study to evaluate the effect of intravenous Dexmedetomidine and clonidine on the characteristics of subarachnoid block by Bupivacaine in Trans-Abdominal Hysterectomy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 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
- Female
入选标准
- •ASA grade I and grade II.
排除标准
- •ASA grade III or above BMI > 30kg/m2 Who will refuse to give consent for spinal anaesthesia History of cardiac rhythm like bradycardia or A-V junction bkock History of preoperative intake of ACE inhibitors, calcium channel blockers, beta blockers, alpha 2 adrenergic receptor antagonist.
结局指标
主要结局
To Evaluate of the effect of Intravenous Dexmedetomidine and Clonidine on the characteristics of Subarachnoid block by Bupivacaine in Trans-Abdominal Hysterectomy
时间窗: 1min, 2mins, 5mins, 10mins, 15mins, 30mins, 45mins, till end of surgery
次要结局
- To determine the hemodynamic consquence of IV Dexmedetomidine and Clonidine administration(1min, 2mins, 5mins, 10mins, 15mins, 30mins, 45mins, till end of surgery)
研究者
研究点 (1)
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