ISRCTN78140744已完成不适用
Oral nifedipine versus intravenous labetalol hydrochloride for acute blood pressure control in hypertensive emergencies of pregnancy: a double blind randomised clinical trial
niversity of Malaya Medical Centre (Malaysia)0 个研究点目标入组 50 人开始时间: 2011年3月17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
- 50
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. Sustained severe hypertension defined as systolic blood pressure of greater than or equal to 160 mmHg and/or diastolic blood pressure greater than or equal to 110 mmHg on at least two occasions in the last 4 hours, at least 30 minutes apart. The latest blood pressure reading must fulfil the criteria of severe hypertension.
- •2. Medical decision to rapidly control blood pressure
- •3. Greater than or equal to 24 weeks gestation
- •4. Viable singleton foetus with acceptable cardiotocography (CTG)
- •5. Maternal heart rate greater than or equal to 60 bpm and less than or equal to 120 bpm
- •6. Aged 19 - 40 years, all pregnant females
排除标准
- •1. Maternal history of cardiac arrhythmia
- •2. Heart failure
- •4. Allergy or contraindication to either nifedipine or labetalol hydrochloride
- •5. Antihypertensive drug treatment in the last 72 hours
研究者
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