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临床试验/NCT02426177
NCT02426177Unknown3 期

Comparison of Oral Labetalol and Oral Nifedipine for Postpartum Hypertension Management

Dow University of Health Sciences0 个研究点目标入组 98 人开始时间: 2015年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
入组人数
98
主要终点
Blood Pressure less than 140/90 mm of hg

研究概览

简要总结

To compare effectiveness of oral labetalol and oral nifedipine for management of postpartum hypertension.

详细描述

A comparison of oral labetalol and oral nifedipine for management of postpartum hypertension. Which drug is more effective in lowering blood pressures in patient with postpartum hypertension.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
20 Years 至 48 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • all women with postpartum hypertension as a continuation of pregnancy induced hypertension,eclampsia, pre-eclampsia or new onset de-novo postpartum hypertension,of any parity.
  • age group between 18-
  • after informed consent.

排除标准

  • all women with chronic hypertension, uncontrolled and un treated medical disorders will be excluded.
  • conditions in which drugs labetalol and nifedipine is contraindicated.

研究组 & 干预措施

group A

Active Comparator

tab.labetalol is given to the patient with postpartum hypertension in dose of 100 mg 6 hourly increased to maximum 600 mg in 24 hours

干预措施: Labetalol (Drug)

group B

Active Comparator

tab.nifedipine is given to the patient with postpartum hypertension in the dose of 10 mg twice a day to maximum dose of 60 mg per 24 hours

干预措施: Nifedipine (Drug)

结局指标

主要结局

Blood Pressure less than 140/90 mm of hg

时间窗: 24 hours

less than 140/90 mm of hg

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

fariha javed

resident

Dow University of Health Sciences

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