A prospective randomised controlled study to determine the effect of bilateral ultrasound- guided Erector Spinae Plane block for postoperative analgesia in cesarean section
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
Dr Benita Abraham
Sri Ramachandra Institute of Higher Education and Research
