PACTR201702002017237已完成未知
Postpartum vaginal blood loss following two different methods of cervical ripening
Okon A Okon0 个研究点目标入组 82 人开始时间: 2017年2月3日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 82
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 Year(s) 至 48 Year(s)（—）
- 性别
- Female
入选标准
- •37 completed weeks up to 41 completed weeks plus 3 days
- •Bishop score of <5
- •a live singleton fetus with cephalic presentation at term
- •intact membranes with no evidence of labor
- •no contraindications to a vaginal delivery
- •up to the third parity
排除标准
- •history of uterine scar
- •breech presentation
- •fetal anomalies
- •antepartum hemorrhage
- •polyhydramnios
- •presence of uterine fibroids in pregnancy
- •known allergy to prostaglandin preparations
- •women with anemia (defined as hemoglobin level less than 10.5g/dl or a hematocrit of less than 31%)
- •bleeding disorders
- •pelvic abnormalities/deformities
研究者
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