NCT00809666已完成不适用
A Prospective Randomised Study of Automated Versus Mercury Blood Pressure Recordings in Pregnancy
St George Hospital, Australia2 个研究点 分布在 1 个国家目标入组 220 人开始时间: 2000年5月1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
- 220
- 试验地点
- 2
- 主要终点
- The primary maternal outcome measure was the number of women having any episode of severe hypertension (BP ³ 170/110mmHg).
研究概览
简要总结
The aim of the PRAM study was to determine whether women diagnosed with hypertension in pregnancy, using the traditional mercury device, have the same pregnancy outcomes when blood pressure is measured by either an automated device or a mercury device throughout the pregnancy.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Single Group
- 主要目的
- Diagnostic
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 16 Years 至 45 Years（Child, Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •women with a diagnosis of hypertension in pregnancy
排除标准
- •non-pregnant and normotensive pregnancy women
结局指标
主要结局
The primary maternal outcome measure was the number of women having any episode of severe hypertension (BP ³ 170/110mmHg).
次要结局
- Secondary end points included gestation at birth, caesarean section and induction of labour rates.
研究者
研究点 (2)
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