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
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