SLCTR/2014/022尚未招募未知
Randomised controlled trial to assess the retention of immediate post-delivery insertion of an intrauterine contraceptive device versus interval intrauterine contraceptive device insertion
District General Hospital, Ampara0 个研究点目标入组 86 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
- 入组人数
- 86
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
入选标准
- •1. Women with planned vaginal deliveries
- •2. Desire for copper IUD insertion
排除标准
- •1. Any contraindications for IUD insertion including infection, hemorrhage and caesarian delivery
研究者
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