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临床试验/CTRI/2024/03/064100
CTRI/2024/03/064100招募中4 期

A multicentric, open label study to evaluate the safety and efficacy of fixed-dose combination of Efonidipine 40 mg and Telmisartan 40 mg tablets in the management of Stage II hypertension. - NI

Zuventus Healthcare Limited0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
招募中

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

入选标准

  • 1. Adults with age 18 years and above 2. Patients diagnosed with Stage II hypertension (SBP/DBP: 160/100 mmHg or above) 3. Naïve patients or patients able to switch from their current antihypertensive therapy without any risk to the patient on the investigator opinion 4. Patients willing to sign informed consent.

排除标准

  • 1. Patients with known hypersensitivity to angiotensin II receptor blockers or dihydropyridine calcium channel blockers
  • 2. Patients with history of severe, malignant or secondary hypertension
  • 3. Patient with cerebrovascular disease in the previous 3 months
  • 4. Patients with chronic arrhythmia, sick sinus syndrome or sinus bradycardia (less than 50 beats per min)
  • 5. Patients with second or third degree atrioventricular block
  • 6. Female patients who are pregnant, lactating

研究者

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