ISRCTN14479515已完成未知
Postpartum vaginal blood loss following two different methods of cervical ripening: a randomised controlled trial
niversity of Calabar Teaching Hospital0 个研究点目标入组 80 人开始时间: 2017年10月16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
- 80
研究概览
简要总结
2017 results in https://pubmed.ncbi.nlm.nih.gov/29410681/ (added 25/11/2020)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. 37 completed weeks up to 41 completed weeks plus 3 days
- •2. Bishop score of <5
- •3. A live singleton fetus with cephalic presentation at term with intact membranes with no evidence of labor
- •4. No contraindications to a vaginal delivery
- •5. Up to the third parity
排除标准
- •1. History of uterine scar
- •3. Breech presentation
- •4. Fetal anomalies
- •5. Antepartum hemorrhage
- •6. Polyhydramnios
- •7. Presence of uterine fibroids in pregnancy
- •8. Known allergy to prostaglandin preparations
- •9. Women with anemia (defined as hemoglobin level less than 10.5g/dl or a hematocrit of less than 31%)
- •10. History of bleeding disorders
- •11. Pelvic abnormalities/deformities
研究者
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