EUCTR2009-013662-33-IT进行中(未招募)不适用
PROSPECTIVE EVALUATION OF SERUM MALDI TOF MS PROTEOMIC PROFILE PREDICTIVE OF OUTCOME IN PATIENTS WITH GLIOBLASTOMA MULTIFORME TREATED WITH STANDARD TREATMENT STRATIFIED ACCORDING TO MGMT - ND
FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR0 个研究点开始时间: 2009年10月2日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
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
- •-C.I. firmato orima di sottoporsi a qualsiasi procedura;eta` compresa tra i 18 e i 70 anni; nuova diagnosi istologica di GBM; etc.
- •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
- •Patient who can not comply with planned protocols procedures
- •Prior chemotherapy within the last 5 years
- •Prior RT of the head
- •Receiving concurrent investigational agents or has received an investigational agent
- •Prior anti-angiogenic therapy
- •Placement of Gliadel? wafer at surgery
- •Planned surgery for other diseases
- •History of malignancy. Subjects with curatively treated cervical carcinoma in situ or basal cell carcinoma of the skin, or subjects who have been free of other malignancies for more than 5 years are eligible for this study
- •Any uncontrolled intercurrent illness (e.g. high blood pressure, unstable angina, serious cardiac arrhythmia, diabetes ), also including severe infection, which may jeopardize the ability of the subject to receive the procedures outlined in this protocol with reasonable safety
- •Subject is pregnant (positive pregnancy test [serum -HCG] at screening), or is currently breast-feeding
- •Any psychological, familiar, sociological, legal or geographical state that could potentially interfere with the study protocol compliance; these conditions should be evaluated before patients enrolment
研究者
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