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临床试验/NL-OMON48975
NL-OMON48975已完成不适用

Flow quantification with ultrasound particle image velocimetry in patients with aortoiliac occlusive disease - echoPIV in AIOD

Rijnstate Ziekenhuis0 个研究点目标入组 120 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
120

研究概览

简要总结

Trial is onging in other countries

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Recently diagnosed untreated aortoiliac stenotic lesion, confirmed with
  • Duplex US (>50%)
  • - Presence of claudication symptoms, but no pain at rest (Fontaine 2a / 2b)
  • - Exercise therapy prescribed,
  • - Recent endovascular treatment of an iliac stenotic lesion through placement
  • of a single stent. Group C:
  • - Recent endovascular treatment of extensive aortoiliac lesion with a CERAB or
  • KS configuration.

排除标准

  • - Hypersensitivity to the active substance(s) or any of the excipients in
  • - Right-to-left cardiac shunt
  • - Severe pulmonary hypertension (pulmonary artery pressure > 90mmHg)
  • - Uncontrolled systemic hypertension
  • - Severe pulmonary disease (e.g. COPD GOLD 3/4, adult respiratory distress
  • - Clinically unstable cardiac disease (recent or ongoing myorcardial
  • infarction, unstable angina
  • at rest, clinically worsening cardiac symptoms, severe cardiac
  • arrythmia*s, etc.)
  • - Loss of renal function (GFR < 45 ml/min)
  • - Congestive heart failure (class III or IV)
  • - Hypersensitivity to iodinated contrast media
  • - Age < 50 (group A)
  • - Pregnancy

研究者

发起方
Rijnstate Ziekenhuis

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