CTRI/2019/03/017917已完成不适用
Efficacy of 0.2% Ropivacaine in surgeon assisted transverse abdominis plane block for postoperative analgesia after caesarean delivery (Performed under spinal anaesthesia)
Chandra Prakash Kalwar1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2017年1月5日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Quality of Analgesia
研究概览
简要总结
To compare the efficacy of 0.2% Ropivacaine in surgeon assisted tratransve abdominis plane block for popostoperative analgesia after caesarean delivery performed under spinal anaesthesia
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 20.00 Year(s) 至 35.00 Year(s)（—）
- 性别
- Female
入选标准
- •Patient giving willful consent.
排除标准
- •Patient Refusal, ASA grade >II, Age<18 years, BMI >35 kg/m2, Complicated pregnancy, Patient with known hypersensitivity to local anaesthetics.
结局指标
主要结局
Quality of Analgesia
时间窗: at VAS 3 or more
次要结局
- Duration of first rescue analgesia(Total dose consumption of rescue analgesia)
研究者
研究点 (1)
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