NCT02714179已完成4 期
A Double Blind Randomised Controlled Trial of Preemptive and Preventive Use of Paracetamol for Pain Relief After Cesarean Section
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 入组人数
- 54
- 主要终点
- Visual analog score (VAS) for pain
研究概览
简要总结
The investigators designed a prospective randomized study to investigate the efficacy of intravenous (IV) preemptive versus preventive paracetamol on postoperative pain scores, patient satisfaction, total morphine consumption and the incidence of morphine-related side effects in patients undergoing cesarean section.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 盲法
- Triple (Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •38 weeks pregnancy, elective cesarean section.
排除标准
- •morbid obesity, cardiac failure, depression.
研究组 & 干预措施
Group Preemptive (Group PE),
Active Comparator
Group I: i.V. paracetamol 1 g (100 ml) was given 30 min before induction of anesthesia.
干预措施: Paracetamol was given intravenously in both group at different times (Drug)
Group Preventive (Group PV),
Active Comparator
Group II: i.V. paracetamol 1 g (100 ml) was given before the end of surgery.
干预措施: Paracetamol was given intravenously in both group at different times (Drug)
结局指标
主要结局
Visual analog score (VAS) for pain
时间窗: 24 hours
次要结局
未报告次要终点
研究者
Ozlem Ozmete
Medical Doctor
Baskent University
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