ISRCTN15346559已完成未知
Process for decision-making, obstetrical RISk management and Mode of delivery After a prior cesarean delivery in Québec (PRISMA): a multicentre, two arms, randomized cluster trial
CHU de Québec Research Center0 个研究点目标入组 24,500 人开始时间: 2015年8月20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
- 24,500
研究概览
简要总结
2017 Protocol article in https://pubmed.ncbi.nlm.nih.gov/28931404/ protocol (added 15/01/2021) 2023 Results article in https://pubmed.ncbi.nlm.nih.gov/38096892/ (added 15/12/2023)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •Hospital level:
- •1. Public hospitals with functional surgical rooms and high performance sonographic devices.
- •2. More than 300 deliveries per year
- •3. Written agreement to participate in the study from the directors of maternity services and professional services
- •Woman level (data collection):
- •1. All women with one prior cesarean delivery who delivered at participating centers and whose newborns had a gestational age of at least 22 weeks and weighed at least 500 g at delivery.
排除标准
- •Hospital level:
- •1. Public hospitals with, at the time of recruitment, recent or ongoing quality-improvement programs specifically designed to target women with one prior cesarean delivery
- •Woman level (data collection):
- •2. Women that give birth or abort before 22 weeks of gestation
研究者
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