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临床试验/CTRI/2026/03/105223
CTRI/2026/03/105223尚未招募4 期

To evaluate and compare the effects of different doses of dexamethasone added to bupivacaine on postoperative analgesia provided by the Transverse Abdominis Plane (TAP) block in patients undergoing lower abdominal surgeries.

Pallavi Mutreja1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2026年3月12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
90
试验地点
1

研究概览

简要总结

This study is a prospective , randomised double blind study which will be conducted to assess and evaluate the efficacy of dexamethasone 4 mg and 8 mg  as adjuvant with bupivacaine in TAP block in 90  ASA I -II patients undergoing elective lower abdominal surgeries . The primary outcome will be the efficacy on postoperative analgesia over first 24 hrs post surgery . The secondary outcome measured will be to determine postoperative opioid consumption in 24 hrs and the adverse effect associated with dexamethasone use.

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
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • ASA I-II scheduled for elective lower abdominal surgeries.

排除标准

  • ASA III and above with coagulopathy diabetes known allergic to local anesthetics and infection at the surgical site.

研究者

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

Pallavi mutreja

World college of medical sciences and research hospital

研究点 (1)

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