ISRCTN89250117已完成未知
A prospective randomized controlled trial (RCT) evaluating the effectiveness of a pharmacological pre-induction and induction of labor protocol using an oral prostaglandin E1 analogue and oxytocin compared to a protocol of mechanical pre-induction and induction of labor using a single-balloon Foley catheter, in and oxytocin in patients scheduled for induction of labor.
Department of Obstetrics and Gynecology, St. Adalbert’s Hospital in Gdansk, Copernicus Healthcare Entity0 个研究点目标入组 300 人开始时间: 2024年1月5日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 300
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
- 性别
- Female
入选标准
- •1. Single live pregnancy
- •2. Cephalic fetal presentation
- •3. No history of previous uterine operations (i.e. cesarean section)
- •4. Indications for induction of labor in accordance with current recommendations of the Polish Society of Gynecologists and Obstetricians
- •5. Lack of contraindications to vaginal delivery
- •6. Confirmed well-being of the mother and fetus
- •7. Informed consent to participate in the study
- •8. Unfavourable cervix
- •9. Full-term pregnancy (>37 weeks of pregnancy)
排除标准
- •1. Presence of uterine scar
- •2. Onset of spontaneous labor
- •3. Premature rupture of membranes (PROM)
- •4. Non-cephalic fetal position
- •5. Multiple pregnancy
- •6. Suspected intrauterine infection
- •7. Contraindications to vaginal delivery and induction of labor following the Polish guidelines
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