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
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
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