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临床试验/CTRI/2017/10/009977
CTRI/2017/10/009977已完成未知

IV Labetalol and Oral Nifedipine in acute control of severe hypertension in pregnancy- A comparative study

Government Siddhartha Medical College0 个研究点目标入组 120 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
120

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

入选标准

  • All antenatal women of gestational age >28 weeks with severe hypertension
  • with systolic blood pressure (BP) of 160 mm Hg or higher and/or diastolic BP
  • of 110 mm Hg or higher on 2 separate occasions 30 minutes apart in lateral
  • recumbent position

排除标准

  • 1. Patients with history of cardiac disease
  • 2. Patients with history of bronchial asthma
  • 3. Patients with history of haematological disorder
  • 4. Patients with history of allergy to labetalol or nifedipine
  • 5. Patients with liver disorders
  • 6. Maternal heart rate <50bpm or >120 bpm
  • 7. Patients with history of exposure to any anti-hypertensive medications in the
  • past 24 hours
  • 8. Patients with chronic hypertension

研究者

发起方
Government Siddhartha Medical College

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