NL-OMON48372已完成不适用
Tonometry (1) and duplex ultrasound (2) to predict Abdominal Aorta Aneurysm (3) progression and cardiovascular events in aneurysm patients - 1-2-3 Trial
Rijnstate Ziekenhuis0 个研究点目标入组 167 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 167
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
- 18 至 99（—）
入选标准
- •1. Male or female at least 18 years old;
- •2. Informed consent form understood and signed and patient agrees to follow-up visits;
- •3. Has an abdominal aortic aneurysm (AAA), who is still under surveillance;
排除标准
- •1. Life expectancy < 2 years;
- •2. Psychiatric or other condition that may interfere with the study;
- •3. Participating in another clinical study, interfering on outcomes;
- •4. Increased risk for coronary spams (score Rose-questionnaire *2);
- •5. Presence of Raynaud*s phenomenon, chronic pain syndrome at upper extremity(s), presence of an AV fistula or shunt, open wounds to the upper extremity(s), and/or scleroderma associated with placing the hand in ice water;
- •6. Recent (<3 months) presence of angina pectoris, myocardial infarction, cerebral infarction, and/or heart failure, or PAD treatment
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