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临床试验/ISRCTN26689999
ISRCTN26689999已完成不适用

A multicentre, randomised trial of primary chemotherapy in inoperable cervical cancer

Cancer Research UK (CRUK) (UK)0 个研究点目标入组 172 人开始时间: 2001年7月1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
172

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 proven invasive squamous cell carcinoma of the cervix uteri
  • 2. Inoperable disease, that is stage II, III or IVA. Stage IIA disease may be included if deemed inoperable by the referring gynaecologist
  • 3. No previous treatment for invasive cervical cancer
  • 4. World Health Organisation (WHO) performance status >2
  • 5. Adequate renal hepatic and haematological function
  • 6. Adequate pulmonary function
  • 7. Patients with a probability of <0.2 of not developing severe encephalopathy with ifosfamide/mensa treatment are excluded
  • 8. Expected survival of >3 months
  • 9. No second primary tumour other than basal cell carcinoma of the skin
  • 10. No other serious medical or psychological condition precluding treatment

排除标准

  • Not provided at time of registration

研究者

发起方
Cancer Research UK (CRUK) (UK)

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