跳至主要内容
临床试验/CTRI/2024/10/075335
CTRI/2024/10/075335尚未招募不适用

Comparison of Intraperitoneal instillation of Bupivacaine with Magnesium sulphate versus Intravenous analgesics drugs for post operative pain relief after Laparoscopic cholecystectomy - A Randomized controlled study .

HERITAGE INSTITUTE OF MEDICAL SCIENCES1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2024年10月24日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
52
试验地点
1
主要终点
To compare post operative pain in laparoscopic cholecystectomy patients who will receive intravenous (IV) analgesics drugs versus those who will receive intraperitoneal Bupivacaine with Magnesium sulphate.

研究概览

简要总结

In this study , 52 patients aged between 20yrs to 60 yrs undergoing laparoscopic cholecystectomy will be randomly divided into 2 groups for comparions of post -op pain relief after laparoscopic cholecystectomy . in one group patient will be given intraperitoneal instillation of bupivacaine with magnesium sulphate ,while in other group patient will receive intravenous analgesic agents for post operative pain.

Measuring indicator : NRS NUMERIC RATING SCALE

RAMSAY SEDATION SCALE

TIME FOR NEED FOR FIRST RESCUE ANALGESIA

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Double

入排标准

年龄范围
20.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Inclusion Criteria
  • Patients undergoing elective laparoscopic cholecystectomy,
  • Patients of ASA grade 1 and 2 and
  • Patients aged between 20 to 60 years.

排除标准

  • Exclusion Criteria
  • Patient who will give negative informed consent .
  • Patients with allergy to the study drugs (MgSO4, Bupivacaine ,Paracetamol)
  • Chronic alcoholics,
  • Patients with heart block or renal failure .
  • Patients with peritoneal drain after surgery.
  • Patients treated with calcium channel blockers.

结局指标

主要结局

To compare post operative pain in laparoscopic cholecystectomy patients who will receive intravenous (IV) analgesics drugs versus those who will receive intraperitoneal Bupivacaine with Magnesium sulphate.

时间窗: AT 30 mins, 1 hour, 2 hour, 3 hour,6 hour, 12hour, 24hour

次要结局

  • To assess changes in hemodynamic response and any adverse effects.(30 mins, 1hour, 2hour,3hour, 6 hour, 12 hour ,24 hour)

研究者

申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Kajal

Heritage institute of medical sciences

研究点 (1)

Loading locations...

相似试验