CTRI/2021/02/031289尚未招募不适用
Comparison of quadratus lumborum block, erector spinae plane block and transversus abdominis plane block for post cesarean section analgesia: A prospective randomized clinical trial.
Dr Aman Malawat1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2021年2月21日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 300
- 试验地点
- 1
- 主要终点
- To compare time of first rescue analgesic needed.
研究概览
简要总结
The aim of this study is to compare the analgesic efficacy of quadratus lumborum block, erector spinae plane block and TAP block in patients who had cesarean section under spinal anesthesia
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Participant, Investigator and Outcome Assessor 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 with ASA Class II, III
- •Normal singleton pregnancy with a gestation of at least 37 weeks
- •Patient’s written and informed consent.
排除标准
- •Patient with ASA Class IV & V
- •Patient refusal
- •Local infection at the site of injection
- •Allergy to study medications
- •Anatomic abnormalities
- •Inability to comprehend or participate in pain scoring system.
结局指标
主要结局
To compare time of first rescue analgesic needed.
时间窗: baseline
次要结局
- To compare the total cumulative dose of analgesic needed in first 48 hours after surgery.(48 hours)
- To compare severity of postoperative pain via visual analogue pain scale at rest (VASR) and with movement (dynamic)(48 hours)
研究者
研究点 (1)
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