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临床试验/CTRI/2025/05/086887
CTRI/2025/05/086887尚未招募不适用

Comparison of intravenous ketamine with propofol versus ketamine with dexmedetomidine for procedural sedation in upper GI endoscopy

Peoples College of medical science and research center1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年6月16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
60
试验地点
1
主要终点
Blood pressure variability

研究概览

简要总结

For this study elective  patients for Upper GI endoscopy will be divided in 2 groups for procedural sedation .1 group will be receiving intravenous ketamine with propofol for sedation and the 2nd group will be receiving  ketamine with dexmedetomidine for sedation .Both the groups will then be compared for haemodynamic changes - blood pressure and pulse and Ramsay sedation score and recovery time .ketamine will be the base drug and will be given in a dose of 1 mg/kg  .propofol will be given in a dose of 1 mg/kg  and  a maintenance dose of 0.25 mg/kg while  dexmedetomidine will be given in a dose of 0.5 mcg/ kg and a maintenance dose of 0.1 mcg/ kg .

In case adequate sedation is not achieved ketamine will be given in dose of 0.25 mg/ kg . Patients in both groups will also be assessed for recovery time along with Ramsay sedation score and haemodynamic changes.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 70.00 Year(s)(—)
性别
All

入选标准

  • •American society of Anaesthesiologist grade 1, 2 and 3 Patients for elective UGI Endoscopy.

排除标准

  • •Patients not giving consent ASA grade more than 3 Patients with cardiac risk Patients with shock Patients with severe hepatorenal impairment.

结局指标

主要结局

Blood pressure variability

时间窗: 20 minutes

次要结局

  • Sedation(20 minutes)

研究者

发起方
Peoples College of medical science and research center
申办方类型
Private medical college

研究点 (1)

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