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临床试验/KCT0008610
KCT0008610招募中Unknown

A multi-center, prospective observational study to evaluate the effectiveness of a single-pill combination of amlodipine, losartan, rosuvastatin, and ezetimibe in patients with hypertension and dyslipidemia

Pusan National University Yangsan Hospital0 个研究点目标入组 550 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
招募中
入组人数
550

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
19(Year) 至 o Limit(—)
性别
All

入选标准

  • 1.Patient diagnosed with essential hypertension and primary hypercholesterolemia, scheduled for treatment with a combination medication containing amlodipine, losartan, rosuvastatin, and ezetimibe.
  • 2.Patient diagnosed with essential hypertension or primary hypercholesterolemia, currently receiving treatment with antihypertensive or lipid-lowering medications, planning to switch to a combination medication containing amlodipine, losartan, rosuvastatin, and ezetimibe.

排除标准

  • 1.According to the approval indications, the combination medication containing losartan and amlodipine should not be administered in cases where there are contraindications specified.
  • 2.The statin class medications (such as rosuvastatin, atorvastatin) and ezetimibe should not be administered in cases where there are contraindications specified.
  • 3.Patients with suspected secondary hyperlipidemia or secondary hyperlipidemia, such as nephrotic syndrome, proteinuria, obstructive liver disease, Cushing's syndrome, etc.
  • 4.If the patient has received investigational drugs for clinical trials within 4 weeks prior to the registration date, or plans to participate in other clinical trials during the study period.

研究者

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