DRKS00014081已完成1 期
Oral nifedipine versus labetalol in treatment of postpartum hypertension - antihypertensive in postpartum
prof ob& gyn0 个研究点目标入组 100 人开始时间: 2018年3月12日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized controlled study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 20 Years 至 40 Years（—）
- 性别
- Female
入选标准
- •Women who have hypertension during pregnancy and persist after delivery till discharge of hospital
排除标准
- •Women with history of secondary hypertension
- •Women with eclampsia who need intensive care unit admission and indicated other drugs rather than oral nifedipine and oral labetalol
- •Women who have any contraindication to Nifedipine or labetalol
研究者
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