PACTR202408671139802招募中3 期
A randomized controlled study of effectiveness, maternal and perinatal outcomes in the use of labetalol versus hydralazine in the management of severe pre-eclampsia in Ahmadu Bello university teaching hospital, Zaria.
Sakina Ghazali0 个研究点目标入组 100 人开始时间: 2023年12月17日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 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
入排标准
- 年龄范围
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •1.Severe hypertension (systolic blood pressure of 160mmHg or more and /or diastolic blood pressure of 110mmHg or more) and Proteinuria of 2+ or more as measured by dipstick in a catheter specimen urine sample.
- •2.Pregnancy = 28 weeks gestation.
- •3.Singleton pregnancy.
- •4.Live fetus with normal fetal heart rate.
排除标准
- •1.Medicaldisorderslikeasthma,cardiacfailure,heartblock, cardiac arrhythmias.
- •2.Contraindication or known allergy to hydralazine or labetalol neurological disease.
- •3.Fetal congenital abnormality.
- •4.Women who refuse consent.
- •5.Referrals already on anti-hypertensive.
研究者
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