EUCTR2007-000759-32-IT进行中（未招募）不适用
Evaluation of the efficacy of green tea catechins (Categ Plus) in the chemoprevention of prostatic carcinoma in patients with high grade PIN. A randomised multicentric, double blind clinical study. - ND
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- SOFAR SPA
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
- Male
入选标准
- •1. age > 45 years
- •2. patients with High grade PIN diagnosed by biopsy. it is possible to refer to a previous biopsy (not before 6 months)
- •3. no clinic evidence of prostate cancer
- •4.written consent
- •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
- •1. patients taking 5-alfa reduttase drugd (finasteride, dutasteride)
- •2. patients with other malignances
- •3. diseases of kidney and liver, cardiovascular and haematological disease, pulmonary or neurological, gastroenterologic or endocrine diseases
研究者
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