跳至主要内容
临床试验/CTRI/2021/12/039016
CTRI/2021/12/039016尚未招募不适用

A comparative study of multimodal analgesia with thoracic epidural for laparotomy

Sri Lakshmi Narayana Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2022年3月1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
100
试验地点
1
主要终点
1)To estimate the time of request of first rescue analgesic

研究概览

简要总结

A double-blinded, prospective study with hundred patients will be divided randomly into two groups of fifty each: Group E will be given epidural analgesia, Group M will be given multimodal analgesia for their post-laparotomy period. Both the groups will be monitored for 48 hours postoperatively. The parameters recorded will be blood pressure, pulse rate, saturation, visual analog scale for pain scores every hour. Whenever the visual analog score crosses 4, patients will be given rescue analgesic. The total number of rescue analgesics required in both groups will be recorded for 48 hours postoperatively.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and 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

  • ASA I & II PATIENTS SURGERY DURATION WITHIN 4 HOURS.

排除标准

  • KNOWN ALLERGY/HYPERSENSITIVITY TO DRUGS USED LOCAL SKIN SITE INFECTION COAGULOPATHY PRE-EXISTING ACUTE/CHRONIC PAIN PREVIOUS ABDOMINAL SURGERIES PATIENTS WITH SIGNIFICANT CARDIAC, PULMONARY, HEPATIC DISEASES.

结局指标

主要结局

1)To estimate the time of request of first rescue analgesic

时间窗: 48 hours

2) To estimate the total dose of rescue analgesic consumed in the early postoperative period

时间窗: 48 hours

次要结局

  • To estimate the incidence of hypotension, nausea and vomiting(48 hours)

研究者

发起方
Sri Lakshmi Narayana Institute of Medical Sciences
申办方类型
Private medical college

研究点 (1)

Loading locations...

相似试验