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临床试验/EUCTR2008-003396-52-FR
EUCTR2008-003396-52-FR进行中(未招募)1 期

Randomized phase III study of neoadjuvant chemotherapy followed by surgery vs. concomitant radiotherapy and chemotherapy in FIGO Ib2, IIa > 4 cm or IIb cervical cancer.

European Organisation for Research and Treatment of Cancer0 个研究点目标入组 626 人开始时间: 2010年9月27日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
626

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • - Cervical carcinoma of following histological types: squamous cell carcinoma, adenosquamous cell or adenocarcinoma
  • - FIGO stage Ib2, IIa >4cm or IIb
  • - WHO performance status of 0-2
  • - 18 - 75 years
  • - ANC > 1.5 x 109/l, platelets > 100 x 109/l, bilirubin < 25 µmol/l or < 1.46 mg/dl, creatinine clearance (calculated or measured) > 60 ml/min
  • - Before patient randomization, written informed consent must be given according to ICH/GCP and national/local regulations.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Small cell, clear cell and other rare variants of the classical adenocarcinoma
  • - prior irradiation or chemotherapy
  • - previous or concurrent second malignancy except for adequately treated basal cell carcinoma of the skin
  • - any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial
  • - pregnant

研究者

发起方
European Organisation for Research and Treatment of Cancer

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Randomized phase III study of neoadjuvant... | 临床试验