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临床试验/IRCT2015110924963N1
IRCT2015110924963N1已完成3 期

Comparison of efficacy and patients satisfaction of sub lingual and oral captopril patients with hypertension

Shahrood Islamic Azad University0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
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
no limit 至 no limit(—)
性别
All

入选标准

  • inclusion: blood pressure 160/100 and more than
  • exclusion: evidence of existence of acute ischemic heart disease; chest pain; dynamic change in EKG; heart failure; pulmonary edema; dissection of aorta; encephalopathy due to hypertension; seizure; loss of consciousness; cerebrovascular accident(ischemic , hemorrhagic); acute and chronic renal failure; history of pheochromocytoma; previous history of bilateral renal artery stenosis; pregnancy; hypertension after surgery; diastolic blood pressure >120; history of allergic reaction to captopril.

排除标准

  • 未提供

研究者

发起方
Shahrood Islamic Azad University

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