NCT07685756进行中（未招募）不适用
Cervical Ripening Balloon Compared With Vaginal Misoprostol for Cervical Ripening in Obese Woman at Term
HUDDA Ahmad1 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2026年5月1日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 108
- 试验地点
- 1
- 主要终点
- Less rate of instrumental delivery and c section
研究概览
简要总结
Cervical ripening balloon compared with vaginal misoprostol for cervical ripening in obese woman at term
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •obese women bmi >30, Bishop score <6 at time of ripening Singleton pregnancy Gestational age more than 37 weeks
排除标准
- •pregnancy with fetal demise congenital anomalies, History of uterine surgery In active labour >4 cm dialated Obs complication History of uterine hyper stimulation and uterine rupture Feel malpresentation
结局指标
主要结局
Less rate of instrumental delivery and c section
时间窗: 12 months
Less rate of instrumental delivery and c section in ripening of obese women with cervical folleys as compared to misoprostol at term
次要结局
未报告次要终点
研究者
HUDDA Ahmad
Postgraduate resident
Pakistan Institute of Medical Sciences
研究点 (1)
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