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临床试验/NCT00981552
NCT00981552已完成早期 1 期

Dosimetric Planning Study Comparing IMRT and 4-field Radiotherapy for Definitive Treatment of Cancer of the Cervix

Sunnybrook Health Sciences Centre1 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2008年12月最近更新:
适应症

试验速览

阶段
早期 1 期
状态
已完成
入组人数
55
试验地点
1
主要终点
Reduction in dose to organs at risk

研究概览

简要总结

A theoretical planning study to compare the normal tissue irradiation when using intensity modulated radiotherapy (IMRT) as opposed to standard radiotherapy for the definitive treatment of cervical cancer.

详细描述

Radiotherapy in combination with chemotherapy is the standard treatment of locally advanced cervix cancer, however with traditional techniques large volumes of bowel and bladder are irradiated causing short-term and long-term genito-urinary and gastro-intestinal side effects. IMRT has the potential to conform precisely to the target and spare normal tissues and reduce side effects. However because there are large dose gradients there is the potential to miss the target due to organ motion. Recent studies have documented organ motion and will be used to define the target. Approximately 60 planning scans, previously used to treat patients with cervix cancer, will be used to replan using an IMRT technique and differences in doses to tumour and normal tissues compared.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

性别
Female
接受健康志愿者

入选标准

  • last 60 patients treated definitively for cervical cancer at Sunnybrook Odette Cancer Centre

排除标准

  • no imaging and no anatomical description of disease

结局指标

主要结局

Reduction in dose to organs at risk

时间窗: 6 months

次要结局

  • Target Coverage(6 months)

研究者

申办方类型
Other

研究点 (1)

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