跳至主要内容
临床试验/NCT01648595
NCT01648595终止2 期

Principal Investigator

Mashhad University of Medical Sciences0 个研究点目标入组 70 人开始时间: 2006年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
70
主要终点
decrease pain and duration of the active phase considerably.

研究概览

简要总结

Background: There are two methods of pharmacologic and non- pharmacologic for reducing pain of delivery. It is necessary to be known effect of these drugs on the mother and fetus during labor adverse. Therefore, the purpose of this study was determination of effect of Fentanyl intravenously on pain severity during the active phase of labor.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
21 Years 至 37 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • multiparas pregnant women (gravid 2-7),
  • term singleton pregnancy,
  • cephalic presentation,
  • low risk pregnancy with no history of drug tolerance (addiction),
  • medical and mental diseases.

排除标准

  • Respiratory rate ≤ 8 or maternal bradycardia (pulse rate less than 60).

研究组 & 干预措施

Fentanyl

Experimental

In case group, 50 micrograms fentanyl was prescribed in two doses with an interval of 1 hour. In control group was not intervention.

干预措施: Fentanyl (Drug)

结局指标

主要结局

decrease pain and duration of the active phase considerably.

时间窗: up to 8 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nahid Jahani Shoorab

Faculty of Midwifery

Mashhad University of Medical Sciences

相似试验

Effect of Fentanyl on Pain Severity and Duration of... | 临床试验