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临床试验/IRCT20200723048182N1
IRCT20200723048182N1招募中3 期

Comparison and Evaluation of the Effect of Oral Captopril and Carvedilol in Patients with Hypertension Urgency.

Islamic Azad University0 个研究点目标入组 70 人开始时间: 待定最近更新:
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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