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临床试验/CTRI/2026/03/105501
CTRI/2026/03/105501尚未招募4 期

Comparison Of The Effect of Intravenous Infusion of Dexmedetomidine And Lidocaine Intraoperatively On Postoperative Analgesia In Patients Undergoing Laparoscopic surgeries

Shivani Meswani1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2026年4月1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
66
试验地点
1

研究概览

简要总结

This study is a prospective randomized single blind comparative clinical study conducted at the Department of Anesthesiology at Dr DY Patil Medical College and Hospital Pune

1-2.pdf None

The aim of the study is to compare the effect of intravenous infusion of dexmedetomidine and lidocaine given during surgery on postoperative pain relief in patients undergoing elective laparoscopic surgeries

A total of 66 patients aged 18 to 60 years with ASA grade I or II will be included and divided into two groups of 33 each. One group will receive dexmedetomidine infusion and the other group will receive lidocaine infusion during surgery

The study will assess postoperative pain scores time to first rescue analgesia total analgesic consumption in 24 hours intraoperative heart rate and blood pressure opioid requirement sedation levels and any side effects

All patients will receive standard general anesthesia. Pain will be assessed using the Visual Analog Scale and sedation will be assessed using the Ramsay Sedation Score. Statistical analysis will be done using appropriate tests

The objective is to determine which drug provides better postoperative analgesia with stable hemodynamics and fewer side effects in laparoscopic surgeries

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 60.00 Year(s)(—)
性别
All

入选标准

  • Patients with ASA grade 1 and 2 Patients scheduled for elective laparoscopic surgeries surgeries under general anesthesia Patients with no known allergy or contraindication to dexmedetomidine lidocaine or other study medications.

排除标准

  • Known hypersensitivity or allergy to dexmedetomidine lidocaine or any other component of the study drugs ASA grade 3 or above Severe hepatic renal or cardiovascular dysfunction History of arrhythmias conduction abnormalities or on antiarrhythmic medications Pregnant or lactating women History of chronic pain opioid use or regular analgesic intake within the past 48 hours Patients with neurological or psychiatric disorders that may interfere with pain perception or assessment Body mass index more than 35 Intraoperative conversion from laparoscopic to open surgery.

研究者

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

Shivani Shailesh Meswani

Dr. D.Y. Patil Medical College, Hospital and Research Centre

研究点 (1)

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