跳至主要内容
临床试验/ISRCTN14141270
ISRCTN14141270已完成不适用

A randomised controlled trial of educational counseling on the management of women who have suffered suboptimal outcomes during childbirth

Hong Kong Health Services Research Fund (Hong Kong)0 个研究点目标入组 180 人开始时间: 2002年10月9日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
180

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

性别
Female

入选标准

  • •Parturients who developed suboptimal outcomes during pregnancy. Suboptimal outcomes are defined as:
  • •1. Perinatal deaths (intra-uterine death, stillbirth and neonatal death)
  • •2. Treatment in the neonatal intensive care unit and special care unit
  • •3. Unexpected obstetric events, which include significant antenatal complications, such as hypertension and ante-partum haemorrhage, and intra-uterine and post-partum events, such as emergency caesarean deliveries, operative vaginal deliveries and haemorrhage

排除标准

  • •Does not meet exclusion criteria

研究者

发起方
Hong Kong Health Services Research Fund (Hong Kong)

相似试验