JPRN-UMIN000051955已完成Unknown
Prospective observational study to investigate lipid-related residual risks for the patients with acute coronary syndrome who were administrated high-dose strong statin - Investigation of lipid-related residual risks after acute coronary syndrome
适应症
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 入组人数
- 62
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
- 20years-old 至 ot applicable（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •(1) Cases who have a contraindication of rosuvastatin treatment (such as in patients receiving cyclosporine) or requires cautious administration (patients with hypothyroidism or patients planning to use fibrates other than fenofibrate). (2) Cases who have a side effects like muscle pain and poor tolerability to rosuvastatin oral administration. (3) Cases who have already used or have a plan to use other high cholesterol-improving medications (such as evolocumab or ezetimibe) during the observation period. (4) Cases of familial hypercholesterolemia. (5) Cases with chronic inflammatory diseases (autoimmune diseases) or ongoing cancer treatment. (6) Cases with impaired consciousness, general malaise, or severe mental disorders. (7) Other cases who are deemed inappropriate by the investigator.
研究者
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