NL-OMON42670尚未招募不适用
Evaluation of a high-resolution dedicated hanging breast PET guided biopsy device for breast cancer diagnosis. - MAMMOCARE
Antoni van Leeuwenhoek 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
- 尚未招募
- 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
- •-Patients who are referred to the AVL for neo-adjuvant chemotherapy treatment
- •-Histological confirmed breast cancer (stage II/III)
- •-Breast tumour >= 2cm
排除标准
- •- 18F-FDG non-avid primary tumour (SUVmax < 2.5) on conventional hanging breast PET/CT
- •- Breast tumour SUVmax lower than two times the SUVmax of surrounding normal breast tissue on conventional hanging breast PET/CT
- •- Primary tumours located within 2.5 cm distance from the chest wall (selection based on earlier performed mammography, hanging breast MRI or PET/CT).
- •- Active infection (breast or systemic) requiring antibiotics.
- •- Breast implant in affected breast
- •- Blood sugar level more than 10 mg/ml at time of 18F-FDG injection
- •- Anticoagulants usage with International Normalized Ratio (INR) > 2 on the day of biopsy
- •- Pregnancy
研究者
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