跳至主要内容
临床试验/CTRI/2023/12/060675
CTRI/2023/12/060675尚未招募不适用

Evaluation of analgesic efficacy of dexmedetomidine as adjuvant with ropivacaine in usg guided adductor canal block in patients undergoing knee arthroscopic surgeries.

Dr Dharam Singh Meena1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2024年1月20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
90
试验地点
1
主要终点
To compare the quality of post-operative analgesia with respect to the intensity (using Visual Analogue Scale) in patients given ropivacaine with dexmedetomidine versus ropivacaine

研究概览

简要总结

The study is undertaken to evaluate analgesic efficacy of dexmedetomidine as adjuvant to ropivacaine in patients undergoing knee arthroscopic surgeries.Primarily we will be checking VAS score in first 24hr and secondarily we will be seeing requirements of rescue analgesic.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

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

入选标准

  • American Society of anaesthesiologists physical status grade I and II scheduled for laparoscopic cholecystectomy.

排除标准

  • Allergy to amide group of local anaesthetic agent, Significant neurological disease in lower limb, renal disease or psychiatric history, Patient on anticoagulants or known case of bleeding disorder.

结局指标

主要结局

To compare the quality of post-operative analgesia with respect to the intensity (using Visual Analogue Scale) in patients given ropivacaine with dexmedetomidine versus ropivacaine

时间窗: 24 hours after block

次要结局

  • To assess the total requirement of rescue analgesic in both the groups(24 hours after block)

研究者

发起方
Dr Dharam Singh Meena
申办方类型
Other [VMMC and SJH]
责任方
Principal Investigator
主要研究者

Simran Kaur Virk

Indraprastha University

研究点 (1)

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