NL-OMON44829已完成不适用
RandomizEd Controlled Trial for pre-operAtive dose-escaLation BOOST in locally advanced rectal cancer. - RECTAL BOOST study
niversitair Medisch Centrum Utrecht0 个研究点目标入组 142 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 142
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99（—）
入选标准
- •* Participant in the PLCRC project (METC 12-510).
- •* Informed consent obtained for being offered experimental interventions within the PLCRC project.
- •* Informed consent obtained for questionnaires on patient reported outcomes within the PLCRC project.
- •* WHO: 0-2.
- •* T3+ (circumferential resection margin (CRM) positive) T4N0-1 or N2 M0-1 (if resectable liver and/or lung metastases).
- •* Referred for chemoradiation.
- •* No contra-indication for MRI.
- •* Tumor distance from ano-rectal transition *10cm.
排除标准
- •* T3 (limited volume / CRM negative).
- •* Inflammatory bowel disease.
- •* Prior pelvic radiotherapy.
- •* At least one contra-indication for capecitabine administration (based on DPD-deficiency, blood count, liver malfunction, renal failure (Creatinine clearance <30ml/min, medical history such as recent cardiac events).
- •* Recent pregnancy *1 year ago.
- •* Inadequate understanding of the Dutch language in speech and/or writing.
研究者
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