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
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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