IRCT20200723048182N1招募中3 期
Comparison and Evaluation of the Effect of Oral Captopril and Carvedilol in Patients with Hypertension Urgency.
适应症
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
- •Refer to the hospital emergency department with symptoms of blood pressure equal to or greater than 160/90 mmHg in patients with hypertension or blood pressure equal to or greater than 180/110 mmHg in patients with new onset of the disease in the age range of 18 to 65 years.
- •Obtaining written consent from patients.
- •Complete the file and information contained in the questionnaire form.
排除标准
- •Failure to obtain written consent from patients
- •Defects in the file and information contained in the questionnaire form
- •Patients with acute chest pain
- •Bradycardia
- •History of heart block or sick sinus syndrome
- •Irreversible heart failure
- •Pulmonary edema
- •Aortic dissection
- •Patients who need intravenous drugs to control blood pressure or require high doses of ACEIs and ARBs (captopril> 50 mg / d, enalapril> 10 mg / d, lisinopril> 5 mg / d, losartan> 50 mg / d, valsartan > 80 mg / d).
- •Loss of consciousness
- •Cerebrovascular accidents (ischemia or bleeding)
- •Acute or chronic renal failure
- •Previous history of pheochromocytoma
- •History of bilateral renal artery stenosis
- •Hypertension after surgery
- •Diastolic blood pressure above 120
- •History of allergies to captopril and carvedilol and allergies to penicillin and sulfonamides.
- •Asthma or other bronchospasm diseases
- •Existence of cardiogenic shock
- •Severe liver failure
- •Papillary edema
研究者
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