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临床试验/CTRI/2015/09/006221
CTRI/2015/09/006221尚未招募3 期

Visibility of strings after post placental insertion of Cu T 380 A and Cu 375 intra uterine contraceptive device: A randomized comparative study.

Safdarjung Hospital0 个研究点目标入组 100 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
尚未招募
入组人数
100

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 fulfilling following criteria will be eligible for study.
  • •1.Women desirous of postpartum contraception for less than or upto 5 years.
  • •2.Women posted for elective / emergency caesarean section
  • •3.Women willing to come for follow up

排除标准

  • •1.More than 18 hours of rupture of membranes before delivery.
  • •2.Any evidence of chorioamnionitis
  • •3.Antepartum hemorrhage or postpartum hemorrhage
  • •4.Fever in recent antepartum period
  • •5.Women in Medical eligibility criteria category 3 or 4 of Copper T insertion.

研究者

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