跳至主要内容
临床试验/EUCTR2005-001139-31-BE
EUCTR2005-001139-31-BE进行中(未招募)1 期

European Paediatric Soft Tissue Sarcoma Study Group protocol for Localized Non-Rhabdomyosarcoma Soft Tissue Sarcomas 2005 - NRSTS 2005

CHC-Clinique Espérance0 个研究点目标入组 250 人开始时间: 2006年6月22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
250

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

  • Eligibility criteria for the prospective non-randomized historically-controlled trial are the following:
  • ?A pathologically proven diagnosis of synovial sarcoma and adult-type soft tissue sarcomas
  • ?No evidence of metastatic lesions
  • ?Age less than 21 years (20 years and 364 days) of age
  • ?No previous treatment except for primary surgery
  • ?For patients who require adjuvant chemotherapy according to protocol guidelines, no more than a 8 week-interval between the diagnostic surgical approach and the start of chemotherapy
  • ?For patients who require adjuvant chemotherapy according to protocol guidelines, no pre-existing illness preventing treatment (in particular renal function must be equivalent to grade 0-1 nephrotoxicity, no prior history of cardiac disease and normal shortening fraction [> 28%] and ejection fraction [> 47%])
  • ?No previous malignancy
  • Patients with post-irradiation soft part sarcomas could be registered and treated according to the protocol guidelines, but they will be analysed separately
  • ?Diagnostic material available for pathology review
  • ?Available for long term follow up through the treatment centre
  • ?Written informed consent for treatment available.
  • Are the trial subjects under 18? yes
  • 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) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Absence of any of the above

研究者

发起方
CHC-Clinique Espérance

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