KCT0007047已完成未知
Single-center Retrospective Confirmatory Clinical study to Evaluate the Efficacy of Retinal-based Cardiovascular Risk Assessment Software as Medical Device (SaMD) DrNoon for CVD
Medi Whale0 个研究点目标入组 1,106 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 1,106
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational Study
入排标准
- 年龄范围
- 20(Year) 至 80(Year)（—）
- 性别
- All
入选标准
- •1. Patients who have been enrolled in the CMERC-HI study (Nov.2013 ~ Jun.2018)
- •2. Patients who have been followed up for 5 years and more or until 31.Dec.2021, or patients who experienced cardiovascular events
- •3. Age 20 ~ 80
排除标准
- •1. Cohort of heart failure or cardiac infarction of the CMERC-HI study
- •2. Patients without any retinal photographs
- •3. Patients without any CT data of coronary calcification
- •4. Patients without any Carotid Ultrasound data
- •5. Patients without any pulse wave velocity(PWV) examination
- •6. Patients with missing value at least one of these factors; age, sex, smoking history and past medical history of hypertension or DM or hyperlipidemia
- •7. Cases have difficulty for analysis with DrNoon for CVD: low quality of retinal photographs including turbidity or artefact
研究者
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