ISRCTN74802813已完成未知
A randomised feasibility trial to determine the impact of timing of surgery and chemotherapy in newly diagnosed patients with advanced epithelial ovarian, primary peritoneal, or fallopian tube carcinoma
Medical Research Council (UK)0 个研究点目标入组 550 人开始时间: 2006年1月25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
- 550
研究概览
简要总结
2015 Results article in http://www.ncbi.nlm.nih.gov/pubmed/26002111 results
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. Clinical and imaging evidence of a pelvic mass with extrapelvic metastatic disease at presentation
- •2. Randomisation should be carried out within 4 weeks of obtaining clinical and imaging evidence of disease
- •3. Serum Cancer Antigen (CA 125) / CarcinoEmbryonic Antigen (CEA) ratio >25 (if the serum CA 125/CEA is less than or equal to 25 and the serum CEA is above the upper limit of normal, the patient should undergo investigations to exclude gastrointestinal cancer)
- •4. Patient planned to receive carboplatin-based chemotherapy
- •5. Patient fit to undergo protocol treatment and follow-up
- •6. No concomitant or previous malignancy likely to interfere with protocol treatments or comparisons
- •7. Written informed consent of the patient
排除标准
- 未提供
研究者
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