PACTR202010738538062已完成未知
COMPARISON OF INTRAVENOUS LABETALOL AND HYDRALAZINE FOR THE CONTROL OF SEVERE HYPERTENSION IN PREGNANCY: A RANDOMIZED CONTROLLED TRIA
MUHAMMAD Sagir0 个研究点目标入组 120 人开始时间: 2020年9月30日最近更新:
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
- 年龄范围
- 19 Year(s) 至 44 Year(s)(—)
- 性别
- Female
入选标准
- •Consenting pregnant women with severe hypertension in pregnancy with systolic blood pressure (SBP) of at least 160 mmHg and/or diastolic blood pressure (DBP) of at least 110 mmHg.
- •Gestational age of 28 weeks or more which will be determined based on ultrasound scan or last menstrual period.
- •Live singleton fetus with normal fetal heart rate.
排除标准
- •All women with cardiac disease such as heart block, ischaemic heart disease, and hypertensive cardiac disease.
- •History of allergy to either hydralazine or labetalol.
- •Chronic medical disorder such as chronic kidney disease and diabetes mellitus.
- •Women with haemoglobinopathy such as HbSS.
- •Multiple gestation.
- •Preterm labour at gestational age of less than 34 weeks
- •Women who are already on other antihypertensive drugs.
- •Patients with stroke
- •Unconscious patients
- •Patients with HELLP syndrome and liver disease
- •Presence of fetal distress
- •Non consenting women
研究者
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