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临床试验/IRCT20181214041963N2
IRCT20181214041963N2尚未招募未知

Design, Implementation and Evaluation of a plan for Labor and Normal Delivery Based on Evidence-Based Clinical Practice: A mixed methods evaluation design

Ahvaz University of Medical Sciences0 个研究点目标入组 256 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
入组人数
256

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
15 years 至 49 years(—)
性别
Female

入选标准

  • Consent to participate in the study
  • primiparous women
  • singleton pregnancy
  • maternal age 15-49 years
  • gestational age 37 to 42 weeks (based on the first day of the last menstrual period or first trimester ultrasound)
  • cephalic presentation
  • normal fetal heart rate (110 -160)

排除标准

  • history of any incision on the uterus
  • - detection of abnormal dimensions of the pelvis through vaginal examination and examination of ischial spines, obstetric conjugation, sacrum concavity, condition of pelvic wall(s) and pubic arch angle
  • abnormal bleeding
  • epidural anesthesia
  • presence of any abnormalities in soft tissue or Bony birth canal (diagnosed through vaginal examination)
  • having an abnormal fetus or intrauterine growth restriction
  • indication for cesarean section (fetal distress, prolapse of the umbilical cord, diagnosis of absolute pelvic stenosis by the doctor)
  • known medical diseases based on the patient's file including history or current suffering from any systemic disease such as diabetes, high blood pressure, heart disease, kidney disease, nervous disease, liver disease, digestive disease, respiratory disease, thyroid disease)
  • Fetal membranes that have been ruptured for more than 8 hours
  • High-risk pregnancy (preeclampsia, placenta previa, Placental abruption, chorioamnionitis, placenta accreta)

研究者

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