跳至主要内容
临床试验/CTRI/2017/11/010699
CTRI/2017/11/010699已完成未知

m-CTG: A low cost mobile-phone cardiotocograph device for antenatal and intrapartum monitoring to prevent perinatal mortality in low resource settings

Grand Challenges Canada0 个研究点目标入组 910 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
910

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • Inclusion criteria
  • 1. Group 1: Pregnant women admitted for delivery
  • 1.1. Inclusion criteria
  • 1.1.1 Age: >18 years ââ?¬â?? 45 years
  • 1.1.2 Parity: any
  • 1.1.3 Gestation age: 37 weeks to 41 weeks
  • 1.1.4 Fetus: Singleton
  • 1.1.5 Risk status: low risk
  • 1.1.6 Labour status: in active labour in first stage of labour of spontaneous onset
  • 2. Group 2. Pregnant women with high risk factors in third trimester
  • 2.1 Inclusion criteria
  • 2.1.1 Age: >18 years ââ?¬â?? 45 years
  • 2.1.2 Parity: any
  • 2.1.3 Gestation age: ââ?°Â¥ 32 weeks
  • 2.1.4 Fetus: Singleton
  • 2.1.5 Labour status: not in active labour

排除标准

  • Exclusion criteria
  • 1. Group 1: Pregnant women admitted for delivery
  • 1.2.1 Women with age outside the range
  • 1.2.2. Women with gestation status outside the range
  • 1.2.3 Women with high risk factors (hypertension, IUGR, oligohydramnios, gestational diabetes, known fetal malformations, multiple gestations)
  • 1.2.4 Women with a medical/systemic disease (cardiac, neurological, respiratory any other systemic disease other than those listed in high risk obstetric condition)
  • 1.2.5 Women with induced labour
  • 1.2.6 Women on drugs at the time of screening/ taken in last 24 hours (tocolytic drugs)
  • 1.2.7 Not given written informed consent
  • 2. Group 2. Pregnant women with high risk factors in third trimester
  • 2.2 Exclusion criteria
  • 2.2.1 Women with age outside the range
  • 2.2.2 Women with gestation status outside the range
  • 2.2.3 Women in active labour
  • 2.2.4 Women taken any tocolytic drug in last 24 hours
  • 2.2.5 Not given written informed consent

研究者

相似试验