NCT01394731已完成4 期
Analgesic Effects of Intravenous Acetaminophen on Labor Pain
适应症
干预措施
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 试验地点
- 1
- 主要终点
- Visual analogue scale (VAS) score for pain
研究概览
简要总结
The purpose of this study is to determine whether intravenous paracetamol is effective in treating labor pain.
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
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •American Society of Anesthesiologists physical class I-II
- •term patients (≥ 37 weeks of gestation)
排除标准
- •previous cesarean section
- •hypertension, pre-eclampsia, eclampsia
- •intra-uterine growth retardation
- •intrauterine fetal death
- •morbid obesity (body mass index ≥ 35)
- •allergy to any of the study drugs
研究组 & 干预措施
Paracetamol 1
Experimental
干预措施: Acetaminophen (Drug)
Paraceatmol 2
Experimental
干预措施: Acetaminophen (Drug)
Meperidine
Active Comparator
干预措施: Meperidine (Drug)
结局指标
主要结局
Visual analogue scale (VAS) score for pain
时间窗: Up to 24 hours
Patients who give written informed consent to participate will be entered into the study. Their VAS score will be determined every hour from the time of randomization until delivery of the baby. This time will vary from one patient to another depending on the duration of labor.
次要结局
未报告次要终点
研究者
研究点 (1)
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