跳至主要内容
临床试验/CTRI/2018/07/014690
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).

RNT Medical College1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2018年2月7日最近更新:

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

申办方类型
Government medical college

研究点 (1)

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