跳至主要内容
临床试验/CTRI/2025/09/094392
CTRI/2025/09/094392尚未招募4 期

To compare efficacy of intravenous ketamine-propofol versus ketamine -dexmedetomidine in adult patient undergoing daycare procedure

Mehak1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年10月2日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
1)To compare the demand of rescue anaesthetic during procedure.

研究概览

简要总结

This study aims to contribute to existing literature by comparing the efficacy of intravenous ketamine- propofol versus ketamine dexmedetomedine in adult patient undergoing daycare procedure .the main focus is to evaluate   the need of rescue bolus required after infusion , time taken to achive adeqaute sedation and effective sedation . through this research , we strive to provide valuable insights aimed at safer and more  efficacious choice for procedural sedation in short surgical procedure.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • ASA Physical status I or II Scheduled for elective daycare procedure willing and able to provide written consent BMI between 18.5 to 29.9 Procedure duration less than 60 minutes.

排除标准

  • known allergy to any of study drug 2)history of cardiovascular, hepatic, renal or psychiatric disorder 3)pregnancy or lactation 4)chronic use of sedative or opioids.

结局指标

主要结局

1)To compare the demand of rescue anaesthetic during procedure.

时间窗: Time from start of infusion to achieve RSS 5 | ( ramsay sedation score ) | from start of infusion , patient movement will be noted. if any movement is seen , that time will be documented.

2)2) To compare time require to achieve adequate and effective sedation for procedure ( Ramsay sedation score 5 ) between the study groups.

时间窗: Time from start of infusion to achieve RSS 5 | ( ramsay sedation score ) | from start of infusion , patient movement will be noted. if any movement is seen , that time will be documented.

次要结局

  • ) To compare the time to eye opening after cessation of infusion of study drugs between study groups.(2) To compare the recovery time between the two study groups)

研究者

发起方
Mehak
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Mehak

Adesh institute of medical science and research

研究点 (1)

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