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临床试验/CTRI/2019/05/019201
CTRI/2019/05/019201尚未招募不适用

Comparision of efficacy of Bupivacaine plus Tramadol with Bupivacaine plus Dexmedetomidine as preincisional infiltration in patients undergoing abdominal surgery under general anaesthesia : A Prospective Randomised Double Blinding Study

Indira Gandhi Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年5月26日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
试验地点
1
主要终点
To compare the efficacy of Bupivacaine plus tramadol vs Bupivacaine plus dexmedetomidine as preincisional infiltration.

研究概览

简要总结

We plan to compare the analgesic effect of pre incisional infiltration of Bupivacaine plus tramadol vs Bupivacaine plus dexmedetomidine in patients undergoing abdominal surgery under general anaesthesia.

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 of ASA physical status 1 and 2 Patients willing to participate Patients undergoing abdominal surgery.

排除标准

  • Patients refusal to participate Patients with pregnancy, morbid obesity, full stomach and emergency surgery Patients with ASA physical status 3 and above.

结局指标

主要结局

To compare the efficacy of Bupivacaine plus tramadol vs Bupivacaine plus dexmedetomidine as preincisional infiltration.

时间窗: From administration of drug to upto 24 hours after surgery

次要结局

  • To compare the post operative effect of analgesia in both groups.(From administration of drug to upto 24 hours after surgery)

研究者

申办方类型
Government medical college

研究点 (1)

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