CTRI/2016/03/006771已完成3 期
Single blinded, randomized, comparative study on the safety and acceptability of PPIUCD insertion using Kellyâ??s forceps and a dedicated PPIUCD inserter
SAID0 个研究点目标入组 500 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 500
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
- •Women who request a PPIUCD insertion during ANC period, at the time of delivery or immediately afterwards, as well as meet overall medical eligibility criteria for the immediate PPIUCD services WHO - IUCD Medical
- •Eligibility Criteria and gives a written and an audio-visual consent as per the protocol.
排除标准
- •Participants with ruptured membranes more than 18 hours prior to delivery.
- •Diagnosis of chorio-amnionitis at the time of delivery.
- •Unresolved postpartum hemorrhage.
- •Beyond 48 hrs postpartum.Undergone caesarean section.
研究者
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