EUCTR2020-000156-35-NL进行中(未招募)1 期
89Zr-Bevacizumab PET/CT imaging of vestibular schwannomas for the prediction of bevacizumab treatment effect in patients with symptomatic neurofibromatosis type 2. - 89Zr-Bevacizumab PET/CT imaging in NF2 patients
eiden University Medical Center0 个研究点目标入组 15 人开始时间: 2020年3月3日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 15
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
- •In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- •-Patients aged 18 years or older
- •-Confirmed diagnosis of NF2 by revised Manchester criteria (appendix C)
- •-Provided written informed consent
- •-Patients must have measurable disease, defined as at least one VS > 0.4 ml (on volumetric analysis) that can be accurately measured by contrast-enhanced T1-weighted cranial MRI scan.
- •-Eligible and planned for bevacizumab treatment
- •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 15
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 15
排除标准
- •A potential subject who meets any of the following criteria will be excluded from participation in this study:
- •-Patients with a contra-indication for PET and MRI, such as pregnancy and metal elements.
- •-Patients with a known allergy to substances used in this study
研究者
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