跳至主要内容
临床试验/CTRI/2019/04/018484
CTRI/2019/04/018484尚未招募不适用

Comparison of ultrasound guided bilateral transversus abdominis plane block versus port site infiltration with ropivacaine for post operative analgesia following laparoscopic cholecystectomy

Dr Umme Sarah1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2019年4月15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
80
试验地点
1
主要终点
Duration of analgesia and Total analgesic requirement in the first 24 hours

研究概览

简要总结

The study is intended to study the effect of Ropivacaine for post operative analgesia in two tehniques, i.e, ultrsound guided transversus abdominis plane block and port site infiltration laparoscopic cholecystectomy surgeries using 0.25% ropivacaine. Here also time for rescue analgesia will be assessed. the sacle used to measure pain is Numerical Rating Score.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

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

入选标准

  • Patients posted for elective laparoscopic cholecystectomy, and ASA 1 and 2 ,.

排除标准

  • Patient not willing to give consent,pregnancy and lactation,Coagulopathy, BMI less than 18 and more than 35, Known allergy to anaesthetic agent,Infection at the site of the block, Alcohol and drug abuse, Patients with chronic pain,Preoperative chronic dependance on opioid medications.

结局指标

主要结局

Duration of analgesia and Total analgesic requirement in the first 24 hours

时间窗: Numerical rating Scale for pain will be assessed serially at 30 mins, 60 mins, 2 hours, 4 hours , 6 hours, 12 hours and 24 hours after the surgery.

次要结局

未报告次要终点

研究者

发起方
Dr Umme Sarah
申办方类型
Other [self]

研究点 (1)

Loading locations...

相似试验