NL-OMON55564招募中不适用
Toxicity prediction in radiotherapy for pelvic cancers, assessing the added value of biological parameters to RT treatment planning variables - StopRTox
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 200
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •-Histologically confirmed urogenital carcinoma (i.e. cervix, uterus, vagina,
- •vulva, prostate, bladder) or rectal cancer
- •-Newly diagnosed patients who are to receive 'radical' EBRT or already treated
- •patients, 6 to 24 months after curative EBRT. (Both patients receiving primary
- •RT and those receiving adjuvant (post-operative) RT are eligible for this study)
- •-Proficient in Dutch
- •-Written informed consent prior to participation
排除标准
- •-Radiotherapy for recurrent disease
- •-Patients with prostate cancer who had prostatectomy or iodine-125
- •brachytherapy
- •-Psychosocial or somatic disorders in the medical history, limiting the
- •possibilities for adequate follow-up
研究者
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