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临床试验/NCT01058759
NCT01058759终止3 期

Taxotere-Enoxaparin-(ENOXA)-Study: 1st-Line Docetaxel-Platin Chemotherapy as Single Therapy or in Combination With Enoxaparin in Patients With Locally Advanced or Metastatic Non-small Cell Lung Cancer, a Phase III Study

Hannover Medical School1 个研究点 分布在 1 个国家目标入组 14 人开始时间: 2009年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
14
试验地点
1
主要终点
Progressive free survival

研究概览

简要总结

Taxotere-Enoxaparin-(ENOXA)-Study: 1st-Line Docetaxel-Platin Chemotherapy as single therapy or in combination with Enoxaparin in patients aged older than 18 years with locally advanced or metastatic non-small cell lung cancer (stadium IIIb/IV), a phase III study. Study hypothesis: Increase of progressive free survival from 5 to 7.5 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Signed informed consent
  • Men and women aged 18 and older
  • Locally Advanced or Metastatic Non-small Cell Lung Cancer stage IIIB/IV without any previous therapy
  • Life expectancy at least 12 weeks
  • EOCG performance < 1
  • Appropriate renal and hepatic function
  • Appropriate Hematology
  • No bleeding events within 4 weeks prior to randomization
  • No indication for prophylactic or therapeutic anticoagulation therapy
  • Appropriate methods of contraception (both: men and women) for women of childbearing potential negative urine pregnancy test within 7 day prior to randomization
  • Capability for s.c. injection of Enoxaparin every 24 hrs

排除标准

  • History of cancer other than NSCLC
  • Known contraindication for Enoxaparin e.g. HIT,
  • Known contraindication for Docetaxel, Cisplatin, Carboplatin or co-medication
  • Participation in any other clinical trials within 30 days prior to randomization
  • Any known medical condition that does not allow therapy according to study protocol
  • Seizure disorder

研究组 & 干预措施

Arm B: Enoxaparin

Experimental

干预措施: Enoxaparin (Drug)

Arm A: No Enoxaparin

Active Comparator

干预措施: No Enoxaparin (Other)

结局指标

主要结局

Progressive free survival

时间窗: monthly

次要结局

  • Overall survival(monthly)
  • RECIST(monthly)
  • Quality of life(every three months)
  • thromboembolic complications(monthly)
  • safety of long term application of Enoxaparin(monthly)
  • overall toxicity(monthly)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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Taxotere-Enoxaparin-(ENOXA)-Study | 临床试验