NL-OMON51865已完成不适用
3D ultrasound of abdominal aortic aneurysm characteristics for predicting aneurysm shrinkage after endovascular repair - 3D US - EVAR
Rijnstate Ziekenhuis0 个研究点目标入组 20 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
- 20
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
- •Age >= 18 years;
- •Unruptured infrarenal or juxtarenal abdominal aortic aneurysm (AAA);
- •Scheduled for elective endovascular repair (EVAR);
- •Preoperative CTA with iodine contrast scheduled or already made;
- •Informed consent form understood and signed.
排除标准
- •BMI>40 kg/m2;
- •Symptomatic AAA;
- •Implanted pacemaker or ICD;
- •Unable to hold breath for <=7 seconds;
- •Pregnant;
- •Hypersensitivity to the active substance(s) or any of the excipients in
- •Known right-to-left cardiac shunt;
- •Severe pulmonary hypertension (pulmonary artery pressure > 90mmHg);
- •Uncontrolled systemic hypertension;
- •Severe pulmonary disease (e.g. COPD GOLD 3 or 4, adult respiratory distress
- •Clinically unstable cardiac disease (recent, < 3 months, or ongoing
- •myocardial infarction, unstable angina at rest, recent percutaneous coronary
- •intervention, clinically worsening cardiac symptoms, severe cardiac
- •arrhythmia*s, endocarditis, etc.);
- •Prosthetic valves;
- •Loss of renal function (GFR < 31 mL/min), end-stage renal disease;
- •End-stage liver disease;
- •Hypercoagulable status, recent (< 3 months) thrombosis;
- •Congestive heart failure (class III or IV);
- •Psychiatric or other condition that may interfere with the study;
- •Participating in another clinical study that interferes on the primary
- •outcomes of this study;
- •3D US measurement of AAA is impossible because of bowel gasses or other
研究者
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