NL-OMON55391招募中不适用
Tonometry(1) and duplex ultrasound(2) to predict cardiovascular events in to be treated patients with an abdominal aortic aneurysm - One-Two-Treat Trial
Rijnstate Ziekenhuis0 个研究点目标入组 194 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
- 招募中
- 发起方
- 入组人数
- 194
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
- •3. Has an infrarenal or juxtarenal abdominal aortic aneurysm (AAA), scheduled
- •for elective repair (i.e open repair, EVAR, FEVAR and CHEVAR) according to
- •standard practice
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 spasms (score Rose-questionnaire >=2);
- •5. Presence of Raynaud*s phenomenon, Marfan syndrome, 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
- •6. Recent (<3 months) presence of angina pectoris, myocardial infarction,
- •cerebral infarction, and/or heart failure, or PAD treatment.
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