跳至主要内容
临床试验/EUCTR2005-003855-11-DE
EUCTR2005-003855-11-DE进行中(未招募)不适用

Gemcitabine and cisplatin in combination with hyperthermia in patients with locally advanced or metastatic pancreatic cancer as second-line therapy after adjuvant or first-line chemotherapy with Gemcitabine or Gemcitabine combination

Klinikum Großhadern, University of Munich / Medical Director: Prof. Dr. med. Burkhard Götze0 个研究点目标入组 75 人开始时间: 2006年6月21日最近更新:

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
75

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
All

入选标准

  • Histologically confirmed diagnosis of a locally advanced inoperable or intraabdominal (including hepatic) metastatic pancreatic adenocarcinoma with progression under preceding first-line-chemotherapy with Gemcitabine or Gemcitabine combination, or with progress during or after adjuvant chemotherapy with Gemcitabine or Gemcitabine combination
  • Karnofsky Performance status >= 70
  • signed informed consent
  • life expectance of at least 12 weeks
  • sufficient organic function
  • 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

  • Preceding firstline chemotherapy with chemotherapeutic agents other than gemcitabine alone or in combination
  • second malignancy
  • allergy to any of the drugs used
  • active infection
  • polyneuropathy
  • hyperthermia treatment technically not conductable

研究者

发起方
Klinikum Großhadern, University of Munich / Medical Director: Prof. Dr. med. Burkhard Götze

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