NL-OMON48971已完成不适用
SURVive: investigating new imaging criteria for non-operative treatment following neoadjuvant chemoradiation in rectal cancer patients - Novel imaging criteria after neoadjuvant therapy rectal cancer.
Heelkunde0 个研究点目标入组 20 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 20
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
- •Patients with rectal cancer who are eligible for treatment with neoadjuvant
- •chemoradiation
- •Patients treated in the LUMC, HMC, Alrijne or GHZ.
- •Age 18 years and older;
- •Willing to participate in all aspects of the study
排除标准
- •Patients with rectal cancer, receiving chemoradiation as part of the TESAR
- •Diabetes mellitus
- •Claustrofobia (low dose benzodiazepines are allowed);
- •Prior radiotherapy to the pelvis
- •If female and fertile: signs and symptoms of pregnancy or a positive pregnancy
- •test / breast-feeding (a formal negative pregnancy test is not obligatory);
- •Presence of any psychological, familial, sociological or geographical condition
- •potentially hampering compliance with the study protocol and follow-up schedule
- •Contraindications for Magnetic Resonance Imaging
- •Patient has evidence of infection in the 14 days prior to the FDG-PET/CT scan
- •localised to the lower abdomen, pelvic region, lower back, inguinal region;
- •Inability to tolerate lying supine for the duration of an FDG-PET/CT
- •examination (~30min)
研究者
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