ACTRN12620001000998招募中未知
A feasibility study to determine the ability of an intra-uterine device (IUD) insertion device to accurately place an IUD in acute postpartum women.
Michael Stitely0 个研究点目标入组 10 人开始时间: 2020年10月6日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 10
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Prevention
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- Female
入选标准
- •1. Age 18 or older.
- •2. Immediately post vaginal delivery, within 10 minutes of placental delivery.
- •3. Previously expressed desire for PPIUD and has signed study consent documents.
排除标准
- •1. Active uterine infection and no fever in labour.
- •2. Having active sexually transmitted infection or other lower genital tract infection.
- •3. Known to have ruptured membranes for more than 24 hours prior to delivery.
- •4. Known uterine abnormalities e.g., Bicornuate/septate Uterus, uterine myomas,
- •5. Manual removal of the placenta.
- •6. Unresolved postpartum haemorrhage or postpartum uterine atony requiring use of additional oxytocic agents in addition to Active Management of the third stage of labour.
研究者
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