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临床试验/NCT06184139
NCT06184139尚未招募不适用

Effect of Maternal Age and BMI on Induction of Labor Using Oral Misoprostol in Late-term Pregnancies: a Retrospective Cross-sectional Study

University of Palermo1 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2023年12月最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
尚未招募
入组人数
104
试验地点
1
主要终点
Safety and tolerability of misoprostol for induction of labor

研究概览

简要总结

To evaluate the effect of maternal age and body mass index (BMI) on oral misoprostol induction of labor for late-term pregnancies.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Late term pregnancies out of labor,
  • Bishop score < 7

排除标准

  • labor (defined as presence of at least three painful uterine contractions every ten minutes),
  • uterine tachysystole (>5 contractions within 10 minutes for two consecutive 10-minute periods),
  • hypertonic uterus,
  • abnormal CTG,
  • contraindications to vaginal delivery (fetal malpresentation such as breech presentation or transverse situation, fetal macrosomia, abnormally implanted placenta, active genital herpes infection, cervical cancer),
  • patients with parity > 4,
  • medical contraindication to misoprostol (asthma, glaucoma),
  • women with previous hysterotomies.

结局指标

主要结局

Safety and tolerability of misoprostol for induction of labor

时间窗: 290 days of pregnancy

Efficacy induction of labor for late term pregnancies according to age and BMI

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

Andrea Etrusco

Principal investigator

University of Palermo

研究点 (1)

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