跳至主要内容
临床试验/ISRCTN48397858
ISRCTN48397858已完成不适用

A randomised trial of maintenance weekly paclitaxel versus observation following remission with first-line induction carboplatin and paclitaxel for patients with ovarian cancer

The Institute of Cancer Research (UK)0 个研究点目标入组 1,200 人开始时间: 2002年10月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
1,200

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
Female

入选标准

  • 1. Histologically confirmed epithelial ovarian cancer, fallopian tube cancer and primary peritoneal cancer
  • 2. Female, aged 18 years and over
  • 3. International Federation of Gynecology and Obstetrics (FIGO) stage III to IV. Receive six cycles of carboplatin/paclitaxel, three-weekly at registration
  • 4. Able to complete quality of life questionnaires
  • 5. Can comply with follow-up requirements. Written informed consent
  • 6. Response to induction treatment (as demonstrated by a Computed Tomography [CT] scan)

排除标准

  • 1. Patients with peritoneal carcinomatosis of 'uncertain' origin which is mucin-secreting
  • 2. Histological evidence of an origin in the gastrointestinal tract, bilary system or lung

研究者

发起方
The Institute of Cancer Research (UK)

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