跳至主要内容
临床试验/CTRI/2020/08/027229
CTRI/2020/08/027229尚未招募1/2 期

Comparison of postoperative analgesic effectiveness of Transverses Abdominis Plane (TAP) Vs Quadratus Lumborum (QL) block in patients undergoing Lower segment caesarean section: a randomised control trial

Departmental funds1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2020年8月23日最近更新:

试验速览

阶段
1/2 期
状态
尚未招募
发起方
入组人数
80
试验地点
1
主要终点
Pain control in both the groups will be compared and is the primary objective

研究概览

简要总结

Multimodal pain management is the standard of care in the surgical patients in the post operative period. LSCS is considered as one of the most common surgeries the practice of the obstetrics. Opioids and other NSAIDs as the analgesics of choice ,have many adverse effects. Hence, establishing different methods other than conventional methods for post op analgesia are the current trend in practice of preoperative care. TAP blocks thoracic sensory nerves T7 - T12 with conventional approach and controls postoperative incisional pain. QLB can control the somatic pain after major abdominal surgery which can be performed in patients undergoing LSCS. It is also considered as an easily approached peripheral nerve block. The studies have shown that it is more or equally effective as TAP block. The prolongation of the duration of analgesia is always an added benefit to the patients.

研究设计

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

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
Female

入选标准

  • Intervention will be given to all patients undergoing LSCS under GA/SAB on odd days and control group will be considered on even numbered days Intervention arm: Patients will receive USG guided bilateral QL block Control Arm; Patients will receive USG guided bilateral TAP block.

排除标准

  • Patients undergoing emergency LSCS Contrindications for SAB Allergic to Local Anaesthetics Patients of chronic pain syndrome.

结局指标

主要结局

Pain control in both the groups will be compared and is the primary objective

时间窗: Numeric rating scale is used to measure pain at 30min, 2hr,4hr, 6hr,12hr and 24hr

次要结局

  • 1. Duration of post operative analgesia and rescue analgesia with tramadol(2. Number of patients requiring rescue analgesia)

研究者

发起方
Departmental funds
申办方类型
Research institution

研究点 (1)

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