NCT02062320已完成不适用
Establishment and Evaluation of a Post Caesarean Acute Pain Service
Brno University Hospital1 个研究点 分布在 1 个国家目标入组 407 人开始时间: 2009年10月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 407
- 试验地点
- 1
- 主要终点
- Visual Analogue Scale (VAS)
研究概览
简要总结
The aim of this study is to compare the efficacy of analgesic methods after Caesarean Section before and after Post Caesarean Acute Pain Service establishing.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Caesarean Section performed from October 2009 to October 2011 (study period)
- •completed "Evaluation of postoperative analgesia after Caesarean Section" form.
排除标准
- •Not completed "Standard Evaluation of postoperative analgesia after Caesarean Section" form.
结局指标
主要结局
Visual Analogue Scale (VAS)
时间窗: 72 hours after Caesarean Section (CS)
Comparison of pain intensity (Visual Analogue Scale (VAS)) during the postoperative period (72 hours) between the two groups according to postoperative analgesic method and method of anaesthesia.
次要结局
- VAS score above 4(72 hours after CS)
- Additional Analgesic Requests (AAR) Count(72 hours after CS)
- Analgesia related complication Rate(72 hours after CS)
研究者
Petr Štourač, MD
MD, Ph.D.
Brno University Hospital
研究点 (1)
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