NCT04490980Unknown不适用
The Analgesic Effect of Butorphanol After Cesarean Section
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 入组人数
- 100
- 主要终点
- change from Visual Analogue Score for pain
研究概览
简要总结
We evaluated the clinical effect of Butorphanol on postoperative analgesia by observing the vital signs of patients, general condition of newborns and pain assessment.
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
- Single (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
- •Healthy women at term (37 to 42 weeks of gestation), who desired cesarean section were eligible to participate. undergoing ；No drug sensitive history
排除标准
- •Patients with a history of anesthetics allergy and patients with preterm labor, multiple pregnancies and severe obstetric complications
研究组 & 干预措施
Observed group
Experimental
干预措施: butorphanol (Drug)
结局指标
主要结局
change from Visual Analogue Score for pain
时间窗: assess VAS at 24 hours, 25 hours, 26 hours, 27 hours, 30 hours, 36 hours after the cesarean section
VAS is the most common pain scale for quantification. The score is higher, the patient will be more painful. That will indicate if the analgesia is effective. Visual analog scale (VAS) ranging from 0 to 10 (with 10 representing the worst pain imaginable) to measure the degree of pain for participants
次要结局
- jaundice index of the newborn,1 minute and 5 minutes Apgar score(jaundice index: 24 hours, 48 hours, 72 hours after the cesarean section)
- blood pressure(at 24 hours, 30 hours, 36 hours after the cesarean section)
- pulse(at 24 hours, 30 hours, 36 hours after the cesarean section)
- heart rates(at 24 hours, 30 hours, 36 hours after the cesarean section)
- breath(at 24 hours, 30 hours, 36 hours after the cesarean section)
研究者
Deng Dongrui
professor,chief doctor
Tongji Hospital
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