EUCTR2014-002226-13-DK进行中（未招募）1 期
A multimodality imaging approach for early detection and prediction of cardiotoxicity in Doxorubicin-treated patients with malignant lymphom - Advanced imaging for identifying doxorubicin-induced cardiotoxicity in lymphoma patients
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 100
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •-Newly diagnosed Hodgkin or non-Hodgkin lymphoma
- •-Intended curative chemotherapeutic treatment including doxorubicin
- •-Age > 18 years
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 70
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 30
排除标准
- •-Planned mediastinal radiation therapy involving the heart (patients receiving only upper mediastinal radiation therapy can still participate)
- •-Previous chemotherapeutic treatment
- •-Previous mediastinal radiation therapy
- •-Pre-existing HF of any cause (LVEF < 50%)
- •-Significant renal disease (eGFR measured within 3 weeks prior to start of chemotherapy should be > 30ml/min/1.73 m2)
- •-Impaired liver function (bilirubin > 20 µmol/l)
- •-Contraindications for MR scan (severe claustrophobia, implanted metallic foreign bodies etc.)
- •-Contraindications for PET scan (adenosine intolerance, 2nd or 3rd degree AV block, long QT syndrome, unstable angina pectoris, sinus node dysfunction)
- •-Unwillingness to participate
- •-Unable to give informed consent or unlikely to comply with follow-up
研究者
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