NL-OMON25377已完成不适用
Evaluation of workflow improvements of new software solution to be used during coronary interventions
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 90
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
入选标准
- •Subject will be undergoing a percutaneous coronary angiography or intervention
- •-Subject is 18 years of age or older, or of legal age to give informed consent per national law
排除标准
- •-Subject participates in a potentially confounding drug or device trial during the course of the study. Co-enrollment in concurrent trials may be allowed provided that pre-approval is obtained from Philips.
- •-Subject meets an exclusion criteria according to national law (e.g. age, pregnant woman, breast feeding woman).
研究者
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