ISRCTN42613663已完成2 期
Establishing the efficacy of advanced semi-automated functional magnetic resonance (MR) imaging in the early prediction of response of locally advanced breast cancer to neoadjuvant chemotherapy: a pilot study
Hull and East Yorkshire NHS Trust (UK)0 个研究点目标入组 52 人开始时间: 2009年6月17日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 52
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
- 性别
- Female
入选标准
- •1. Provide written informed consent
- •3. Aged 18 years or over
- •4. Newly diagnosed, histologically proven breast cancer (TNM stage T2- T4B, N0-3C, and M0)
- •5. Undergone both x-ray mammography and breast ultrasound scanning during the current treatment episode
- •6. Scheduled for neo-adjuvant chemotherapy
排除标准
- •1. Are medically unstable
- •2. Previously undergone chemotherapy
- •3. Have had surgery or radiotherapy for cancer in the ipsilateral breast
- •4. Have had surgery to the ipsilateral breast within the previous 4 months for benign breast disease
- •5. Have a history of serious breast trauma within the last 3 months
- •6. Are pregnant or breast feeding
- •7. Have renal failure
- •8. Fail the normal safety requirements of MR, particularly pacemakers and cardiac defibrillators
- •9. Are known to have had an allergic reaction associated with previous administration of a paramagnetic contrast agent
- •10. Have a known contraindication to MR scanning
- •11. Have a disability preventing MR scanning in the prone position
- •12. Have body habitus incompatible with MR system entry
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