ISRCTN10169595已完成未知
Does intraoperative use of the MarginProbe device reduce the need for further re-excision procedures after conservation surgery for breast cancer?
niversity Hospital of South Manchester0 个研究点目标入组 467 人开始时间: 2017年3月27日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 467
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Women aged 18-90 years with DCIS or Invasive Breast cancer containing DCIS diagnosed histopathologically
- •2. Histologically diagnosed DCIS or invasive lobular cancer in core biopsy (B5a or B5b). Invasive lobular carcinoma does not require concomitant DCIS.
- •3. Tumour size 1.5cm - 4cm and undergoing BCS
- •4. Written informed consent
排除标准
- •1. Unsuitable for BCS on basis of tumour size (>4cm) or stage.
- •2. Radiotherapy contraindicated.
- •3. No histopathological evidence of DCIS or invasive lobular cancer.
- •4. Small invasive cancers (<1.5cm)
- •5. Multicentric Disease (histologically diagnosed cancer in two different quadrants of the breast), unless resected in a single specimen
- •6. Bilateral disease (diagnosed cancer in both breasts)
- •7. Neoadjuvant systemic therapy
- •8. Previous radiation in the operated breast
- •9. Implants in the operated breast
- •10. Pregnancy
- •11. Lactation
- •12. Cryo-assisted localisation
- •13. Patients who are undergoing full cavity excision following removal of the main lumpectomy specimen during initial lumpectomy procedure.
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