跳至主要内容
临床试验/CTRI/2023/11/060025
CTRI/2023/11/060025尚未招募不适用

Study on evaluation of perfusion index as a tool to assess the analgesic efficacy of dexmedetomidine during laparoscopic cholecystectomy under general anaesthesia

Amala Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年11月26日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
试验地点
1
主要终点
Primary outcome - incidence and severity of intra-op pain stimulus assessed using perfusion index tool

研究概览

简要总结

Quantifying nociception under anaesthesia is difficult and therefore reaction to nociception is used for monitoring through increased sympathetic activity or the corresponding decreased sympathetic stimulation

In any way surgical procedures as far as an anaesthetist is concerned in providing pain free journey is most important. So to identify nociceptive condition as fast as possible via an effective simple reliable tool is important. The usual parameters we use for pain assessment is heart rate, blood pressure variation and in this study we are assessing whether perfusion index can assess the nociceptive changes in surgery in an effective and reliable way.

In this study we mainly aim at comparing the parameters used for assessing pain like heart rate, systolic blood pressure, diastolic blood pressure, mean arterial pressure along with variations of perfusion index in patients receiving dexmedetomidine infusion intra operatively and patients receiving conventional anaesthesia for laparoscopic cholecystectomy procedures.

After meeting inclusion and exclusion criteria a total number of 60 patients will be recruited for this longitudinal study in a consecutive sampling manner.

Primary objective of study is to compare the variation in perfusion index in response to pain stimulus and variability of perfusion index in subsequent pain stimulus after intravenous administration of dexmedetomidine during laparoscopic cholecystectomy surgeries under General anaesthesia and to compare the perfusion index with hemodynamic parameters such as heart rate, systolic blood pressure, diastolic blood pressure, mean arterial pressure with or without dexmedetomidine

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

  • Physical state ASA 1-2 Age group 18 years to 70 years Patients undergoing elective laparoscopic cholecystectomy surgeries under General anaesthesia.

排除标准

  • Patients not willing to participate in this study History of allergy to the drugs in the study Patients with neurological or psychiatric illness,chronic pain disorder.

结局指标

主要结局

Primary outcome - incidence and severity of intra-op pain stimulus assessed using perfusion index tool

时间窗: Before induction,after induction,after intubation,1,2,3,2,4,6,8,10,15,20,25,30 minutes

次要结局

  • Comparison of perfusion index with hemodynamic parameters like heart rate, systolic blood pressure, diastolic blood pressure and mean arterial pressure(Before induction, after induction, after intubation,1,2,3,2,4,6,8,10,15,20,25,30 minutes)

研究者

申办方类型
Private medical college

研究点 (1)

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