IRCT20200722048172N1招募中3 期
Comparison and evaluation of the effectiveness of oral captopril and oral hydrochlorothiazide in the treatment of urgency hypertensive patients
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 入组人数
- 70
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
- 18 years 至 65 years(—)
- 性别
- All
入选标准
- •Patients with known hypertension with a blood pressure of 160/90 mm Hg or more and patients with the new-onset sever hypertention with a blood pressure of 180/110 mm Hg or more without organ damage (urgency) will be included in the study if satisfied.
- •Patients between the ages of 18 and 65 will be included in the study.
排除标准
- •Patients who need intravenous drugs to control their blood pressure or other blood pressure medications for different reasons.
- •Patients who need high dose of ACEIs or ARBs (> 50 mg/d Captopril, > 10 mg/d Enalapril, > 5 g/dLisinopril, > 50 mg/d Losartan, > 80 mg/d Valsartan),to control their blood pressure.
- •Patients with myocardial infarction presenting with acute chest pain.
- •Patients with severe renal or hepatic failure,anuria, papillaryedema, pulmonary edema, loss of consciousness, seizure,aortic dissection, or bilateral renal artery stenosis; pregnantpatients, patients with a history of overt allergy or angioedemawith ACEIs, Allergy to penicillins and sulfonamides.
研究者
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