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临床试验/CTRI/2025/08/093575
CTRI/2025/08/093575尚未招募不适用

A Comparative Study Of the Analgesics Efficacy of Ultrasound-Guided Quadratus Lumborum Block(QL) VS Transversus Abdominis Plane (TAP)Block For Patients Undergoing Elective Caesarean Section In a Tertiary Care Hospital A Prospective Randomised Double Blinded Study

Pratheeksha Ballal1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年9月20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
70
试验地点
1
主要终点
Postoperative pain score using Visual Analogue Scale (VAS) at rest and movement over 24 hours

研究概览

简要总结

This study is a prospective randomized double blinded controlled trial being conducted at Sri Sathya Sai Medical College and Research Institute. It aims to compare the analgesic efficacy of ultrasound guided quadratus lumborum block and transversus abdominis plane block in women aged 18 to 40 years with ASA physical status I or II undergoing elective caesarean section under spinal anaesthesia. A total of 70 participants will be randomized into two groups of 35 each. Group QL will receive 20 ml of 0.25 percent bupivacaine bilaterally in the quadratus lumborum block and Group TAP will receive 20 ml of 0.25 percent bupivacaine bilaterally in the transversus abdominis plane block. The primary objective is to compare the duration of effective postoperative analgesia between the two groups using visual analogue scale scores, while secondary objectives include assessing the time to first rescue analgesia, total analgesic consumption, and adverse events. Institutional ethics committee approval has been obtained and written informed consent will be taken from all participants.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 40.00 Year(s)(—)
性别
Female

入选标准

  • 1.Patients falling under ASA physical status I and II 2.Patients under the Age 18 to 40 years 3.Patient with BMI of18 to 35.

排除标准

  • 1.Patients Allergic to local anaesthetics 2.Patients with Seizure disorders 3.Patients with Coagulopathy or anticoagulant therapy 4.Patient with Infection at injection site.

结局指标

主要结局

Postoperative pain score using Visual Analogue Scale (VAS) at rest and movement over 24 hours

时间窗: Pain score (VAS at rest and on movement) at 1, 4, 8, 12, and 24 hours postoperatively

次要结局

未报告次要终点

研究者

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

Pratheeksha Ballal

Shri Sathya sai medical college and research institute

研究点 (1)

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