PACTR202404666076601已完成未知
Transcervical Foley Catheter with a 50-mL versus 80-mL Single Balloon Volume for Cervical Ripening in Late and Postterm Nulliparous Women: A Single Center Randomized Clinical Trial.
Franklin Okumu0 个研究点目标入组 120 人开始时间: 2024年3月14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
- 120
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
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •Nulliparous women (no prior pregnancy > 20 weeks gestation)
- •Aged = 18 years.
- •Gestational age of 41+0 weeks or beyond, based on the last known monthly period.
- •Carrying a single live intrauterine pregnancy in cephalic presentation, with intact amniotic membranes.
- •Demonstrating a reassuring fetal heart rate pattern on cardiotocograph (CTG) tracing.
- •Nonsignificant contractions (two or more in 10 minutes).
- •Unfavourable cervix (Bishop score < 6).
排除标准
- •History of antepartum bleeding.
- •Use of another ripening agent before FC placement.
- •Active lower urinary tract infections.
- •known or suspected latex allergy.
- •Placenta previa.
- •Significant fetal anomalies.
- •Contraindications to vaginal delivery.
- •Known or newly diagnosed human immunodeficiency virus (HIV) infection.
研究者
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