跳至主要内容
临床试验/CTRI/2022/07/044455
CTRI/2022/07/044455尚未招募不适用

Evaluation of postoperative analgesic effect of intraperitoneal instillation of 0.125% levobupivacaine + 1 μg/kg dexmedetomidine or 0.2% ropivacaine +1 μg/kg dexmedetomidine after laparoscopic cholecystectomy.

JLN medical college Ajmer1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年5月8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
1. Duration of post operative analgesia.

研究概览

简要总结

We aimed to conduct a study to evaluate postoperative analgesic efficacy of intraperitoneal instillation of levobupivacaine + dexmedetomidine or ropivacaine + dexmedetomidine in patients undergoing laparoscopic cholecystectomy.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Investigator 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

  • •1.Patient belonging to ASA I and II 2.Gall bladder calculi.

排除标准

  • •ASA grade III and above.
  • •age <18 years and >60 years.
  • •patients with severe systemic disease like IDDM, uncontrolled hypertension, kidney and liver disease, severe respiratory disease.
  • •seizure disorder.
  • •CAD or recent history of MI.
  • •Anticipated difficult intubation.
  • •body weight >100kg or obese.
  • •pregnant and lactating women.
  • •patient of psychiatric disorder and sleep disorders.
  • •10.hypersensitivity to study drugs.
  • •11.conversion of laparoscopic cholecystectomy to open cholecystectomy.

结局指标

主要结局

1. Duration of post operative analgesia.

时间窗: 1. Duration of post operative analgesia at 0,1,2,4,6,8,10,12,24 hours.

次要结局

  • 1.total rescue analgesic required in 24 hours.(2. hemodyanamic changes.)

研究者

发起方
JLN medical college Ajmer
申办方类型
Government medical college

研究点 (1)

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