临床试验/CTRI/2022/03/041080

CTRI/2022/03/041080已完成不适用

Effect of oral clonidine premedication on perioprative hemodynamic response for patients undergoing laparoscopic cholecystectomy

Department of anaesthesia1 个研究点分布在 1 个国家目标入组 100 人开始时间: 2022年1月4日最近更新: 2023年4月15日

试验速览

阶段: 不适用
状态: 已完成
发起方: Department of anaesthesia
入组人数: 100
试验地点: 1
主要终点: intra-operative haemodynamic parameters.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

this study was designed to evaluate the effects of oral clonidine premedication on heamodynamic response and modulation of post-operative pain in patients undergoing laparoscopic surgeries.4

To compare intra-operative haemodynamic parameters.

To compare pain and sedation scores

To compare time of first postoperative analgesia

To compare adverse effects

This prospective randomized, single blind, comparative study was conducted on adult patients undergoing laparoscopic cholecystectomy surgeries

研究设计

研究类型: Interventional
分配方式: Random Number Table
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 of ASA grade 1-2 2)Patients of both sex 3)Patients in age group 18-60 years 4)Patients scheduled for laparoscopic cholecystectomy surgeries.

排除标准

•Patients not fulfilling eligibility criteria 2)Lack of patient consent 3)Drug dependence 4)History of bronchial asthma 5)Patients allergic to clonidine 6)Hypertensive and diabetic patients 7)Severe coronary insufficiency, recent Myocardial infarction 8)Concomitant use of monoamine oxidase inhibitors, tricyclic antidepressantsor opioids.

结局指标

主要结局

intra-operative haemodynamic parameters.

时间窗: Intraoperatively (90-120 minutes)

次要结局

Pain and sedation scores, duration of postoperative analgesia.(Adverse effects)

研究者

发起方

Department of anaesthesia

申办方类型

Government medical college

研究点 (1)

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