CTRI/2015/04/005683招募中4 期
COMPARISON OF INTRAVENOUS LABETALOL,INTRAVENOUS HYDRALAZINE AND ORAL NIFEDIPINEFOR ACUTE BLOOD PRESSURE CONTROL INHYPERTENSIVE EMERGENCIES IN PREGNANCY:A RANDOMIZED DOUBLE BLIND TRIA
niversity College of Medical Sciences and associated Guru Teg Bahadur Hospital0 个研究点目标入组 105 人开始时间: 待定最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 105
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
- •1. Pregnant women beyond 20 weeks gestation or during intrapartum period detected to have a systolic BP more than equal to 160 mm Hg or diastolic BPmore than equal to 110 mmHg will be recruited. These patients could be
- •a. Cases of gestational hypertension with no previous antihypertensive therapy.
- •b. Cases of gestational hypertension with previous antihypertensive therapy other than Labetalol, Hydralazine or Nifedipine
- •c. Cases of gestational hypertension with superimposed pre-eclampsia
- •d. Cases of severe preeclampsia, HELLP syndrome with systolic BP ï?³160 mm Hg and/or diastolic BP >=110 mmHg.
- •2. Women willing to participate in the study with informed written consent.
排除标准
- •1. Eclampsia
- •2. Cases presenting with pulmonary edema
- •3. Cases of severe hypertension in pregnancy with impaired state of consciousness or altered sensorium
- •4. Women with history of heart disease, asthma, renal disease
- •5. Intake of any of the drugs being studied, in preceding 72 hours
- •6. Women presenting with history of allergy to any of the drugs being studied or developing adverse effects requiring discontinuation of therapy
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