ISRCTN17871140进行中（未招募）Unknown
Combined monitoring for hypertensive pregnancy: a feasibility trial
试验速览
- 阶段
- Unknown
- 状态
- 进行中（未招募）
- 入组人数
- 60
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
- •1. Participant is willing and able to give informed consent for participation in the study
- •2. Pregnant women aged 18 years to 60 years
- •3. Diagnosis of hypertension (blood pressure previously sustained at =140/90mmHg)
- •4. From 20 weeks (+/-4 weeks) gestation, up to 34 weeks gestation
- •5. Currently prescribed one antihypertensive medication
- •6. Currently negative protein on urine dipstick testing
排除标准
- •1. Women whom the midwife or obstetrician feels that it would be inappropriate to approach, for example, those acutely unwell
- •2. Participant does not wish to self-monitor / self-manage their blood pressure
- •3. Abnormal uterine artery Doppler results in this pregnancy
- •4. Early onset (<34 weeks gestation) pre-eclampsia in a previous pregnancy
- •5. Imminent delivery
研究者
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