跳至主要内容
临床试验/CTRI/2024/05/067919
CTRI/2024/05/067919已完成3 期

A prospective randomised controlled study to determine the effect of bilateral ultrasound- guided Erector Spinae Plane block for postoperative analgesia in cesarean section

Dr Benita Abraham1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年6月7日最近更新:

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
Visual analog scale (VAS) for pain

研究概览

简要总结

We are conducting a study in patients who are undergoing cesarean section to compare Erector spinae block against standard analgesia . Erector Spinae Plane block is used to reduce pain after surgery. We will collect data from participants after the procedure to compare both regimes and see which is providing more effective analgesia and is better tolerated . This data will help us in future to choose and provide good anesthesia for other patients. It’s is a PROSPECTIVE RANDOMIZED CONTROLLED , SINGLE BLIND STUDY.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
Female

入选标准

  • Undergoing Cesarean Section.

排除标准

  • Patient refusal to ESPB presence of coagulopathy or bleeding disorder were administered an antiplatelet agent local infection at the injection site hypersensitivity to local amide anesthetics central neuropathy uncontrolled diabetes mellitus significant cardiopulmonary disease, hepatic or renal failure or psychiatric disease.
  • Inability to give consent to the study.

结局指标

主要结局

Visual analog scale (VAS) for pain

时间窗: 0 hour, 2 hours , 4hours, 6 hours , 8 hours, 12hours 24 hours and 48 hours

次要结局

  • Total postoperative analgesia
  • Time for the first request to analgesia(Hours)
  • Incidence of adverse effects(Number of events in 48 hours)

研究者

发起方
Dr Benita Abraham
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Benita Abraham

Sri Ramachandra Institute of Higher Education and Research

研究点 (1)

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