Efficacy and Satisfaction With Remifentanil Analgesia in Parturients During the Childbirth: Retrospective Observational Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 66
- 试验地点
- 2
- 主要终点
- Efficacy of remifentanyl analgesia during the delivery
研究概览
简要总结
Retrospective observational study to determine the efficacy of remifentanil during the delivery. Authors will search the data in period between 2010 and 2014 in cohort of 100 parturients and obtain data of analgesic efficacy (VAS score after remifentanil analgesia induction) and parturients satisfaction with the method.
详细描述
In retrospective observational study will authors search the documentation of parturients. The cohort size is estimated to 100 subjects, in period between 2010-2014. Excluded will be all patients who did not signed the informed consent for processing with their medical data.The main aim is to evaluate the efficacy of the remifentanil analgesia in parturients in the first phase of delivery.
The analgesic efficacy will be evaluated by the change in VAS (visual analogue scale) score after induction of remifentanil analgesia Satisfaction will be evaluated by the questionary.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •parturients during the delivery
- •administered remifentanil analgesia
- •signed informed consent
排除标准
- •informed consent not signed
- •missing data about the analgetic method a analgetic efficacy
研究组 & 干预措施
Parturients with remifentanil analgesia
Parturients after induction of remifentanyl analgesia during the delivery
干预措施: remifentanil (Drug)
结局指标
主要结局
Efficacy of remifentanyl analgesia during the delivery
时间窗: VAS score before the induction of remifentanyl infusion and 1hour after initiation of remifentanil analgesia during the first phase of delivery
To evaluate the efficacy of remifentanil analgesia during the first phase of delivery in parturients by observing changes in VAS score
次要结局
- Patient satisfaction with analgetic method(Before initiation of anagetic method (first phase of delivery) and 1hour after childbirth)
研究者
Petr Štourač, MD
MD, Ph.D
Brno University Hospital