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临床试验/IRCT20110103005534N2
IRCT20110103005534N2招募中3 期

The effect of intravenous syntocinone injection on the third stage of labor in pregnant women

Shiraz University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 years 至 35 years(—)
性别
Female

入选标准

  • Willingness to participate in the study
  • Term pregnancy (37-42 weeks)
  • Single pregnancy
  • vertex presentation
  • Age 18- 35 years
  • Number of deliveries 0-2
  • Spontaneous onset of labor pains
  • No chronic diseases (heart disease, hypertension and diabetes)
  • Absence of high-risk pregnancies (gestational hypertension, decreased fetal motility, fetal death, amniotic polyhydramnios and oligohydramnios known by ultrasound, rupture of membranes more than 12 hours, history of infertility)
  • alive fetus
  • Birth weight between 4500-2500 grams
  • Prenatal hemoglobin more than 10 grams per deciliter
  • absence of placenta previa
  • absence of placenta abruption
  • No history of any bleeding during pregnancy
  • No curettage history
  • Absence of any scar on the uterus
  • Do not take anticoagulants

排除标准

  • Reluctance to continue participating in the study
  • Disorders in the progress of labor
  • prolong labor (more than 20 hours)
  • precipitate labor( less than 3 hours)
  • Blood pressure of 140/90 mm Hg or more during the study
  • Disorders in labor (prolong labor, dystocia, placenta abruption , umbilical cord prolapse, etc.)
  • Manual Removal of the Placenta
  • Abnormal fetal heart rate patterns leading to cesarean section
  • Lack of progress of labor that leads to cesarean section
  • Expansion of the episiotomy
  • Excessive postpartum hemorrhage (more than 500 cc)
  • Using vacuum
  • postpartum re-manipulation of the perineum

研究者

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