NCT02801968Unknown不适用
Tap Block and Cesarean Delivery: Efficacy and Consumption of Postoperative Drugs
S. Anna Hospital1 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2016年4月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 发起方
- 入组人数
- 62
- 试验地点
- 1
- 主要终点
- Pain evaluation with Numerical Rating Scale (NRS)
研究概览
简要总结
The purpose of this study is to determine the efficacy of Tap block after cesarean delivery as a component of multimodal analgesia and evaluation of postoperative drugs consumption.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •age > 18 years
- •written consent
- •anesthesiologist's assent on preoperative evaluation
排除标准
- •age< 18 years
- •uncooperative patients
- •written consent not obtained
- •local anesthetic allergy
- •BMI > 35
结局指标
主要结局
Pain evaluation with Numerical Rating Scale (NRS)
时间窗: Pain evaluation with NRS at 2,6,12,24 hours after cesarean delivery in TAP block group and in the control group.
We don't want to measure the change between each assessment within a single group, instead we want considering the difference in the measurements between two separate groups (TAP block group and control group) for each time point.
次要结局
- Evaluation of NSAIDs (nonsteroidal anti-inflammatory drugs) consumption as rescue dose during the first 24 hours after cesarean delivery(Doses of NSAIDs (nonsteroidal anti-inflammatory drugs) administered at 2, 6, 12 ,24 hours after cesarean delivery TAP block group and in the control group.)
研究者
Ilaria Farinelli
Doctor
S. Anna Hospital
研究点 (1)
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