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临床试验/CTRI/2019/06/019683
CTRI/2019/06/019683尚未招募不适用

A Comparative study of intravenous Dexmedetomidine and Clonidine on haemodynamic response in laparoscopic lower abdominal onco-surgeries.

PRASHANT HATTI1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2019年6月14日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
48
试验地点
1
主要终点
comparing the hemodynmic responces.

研究概览

简要总结

From the early 1970slaparoscopic procedures became well established because of its advantages likereduced post operative pain, improved cosmesis, reduced hospital stay.

Despite its advantages,laparoscopic surgeries have its own demerits due to pneumoperitoneum andpositional changes. Pneumoperitoneum causes alteration in cardiorespiratoryphysiology like reduced thoracopulmonary compliances, reduced functionalresidual capacity(FRC), increased arterial pressures, increased systemicvascular resistance and pulmonary vascular resistance. Plasma catecholamines and vasopressin levelsincreases during pneumoperitoneum which is associated with changes in totalperipheral resistance. Trendelenburgposition and Carbon dioxide(CO2)causes hemodynamic stress.

Various pharmacologicalagents like nitroglycerine, beta blocker, magnesium sulphate and opioids areused to provide hemodynamic stability during pneumoperitoneum with their ownlimitations.

Alpha-2 (α2)adrenergic agonists have shown the promising result in maintaining the baselinehemodynamic parameters during laparoscopic surgeries with minimal adverseeffects. Alpha-2 (α2) adrenergic agonists are useful in attenuating thehemodynamic responses produced by pneumoperitoneum. But not many studies havebeen done studying the comparative effect of these two drugs especially inlaparoscopic onco-surgeries. Hence this study is being taken up to compare intravenousdexmedetomidine and clonidine on haemodynamic response in laparoscopic lowerabdominal onco-surgeries.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant 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 aged between 18 – 60 years Patients belonging to ASA Grade I and II.

排除标准

  • Patient refusal Patient age below 18 years and above 65 years Patient belonging to ASA grade III and IV Patients on beta-blockers.
  • Patients with cardiac dysfunction, hepatic, renal disease.
  • Patients with psychiatric disorders.
  • Patients with allergic disorders.

结局指标

主要结局

comparing the hemodynmic responces.

时间窗: during intubation, during pneumoperitonium, during extubation.

次要结局

  • comparing the hemodynmic responces.(Every 5 min from intubation till pneumoperitonium, every 10 min from pneumoperitonium till extubation.)

研究者

发起方
PRASHANT HATTI
申办方类型
Other []

研究点 (1)

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