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临床试验/NCT03465501
NCT03465501已完成不适用

Interstitial Brachytherapy Boost for Treatment of Anal Canal Cancers, Comparison of Two Dose Rates

Institut Paoli-Calmettes1 个研究点 分布在 1 个国家目标入组 89 人开始时间: 2007年8月17日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
89
试验地点
1
主要终点
Evaluation of the efficacy of interstitial brachytherapy of the anal canal

研究概览

简要总结

Comparative retrospective study of two anal canal brachytherapy techniques aimed at boosting [low dose rate (LDR) and high dose rate (HDR)]

详细描述

Efficacy of anal canal interstitial brachytherapy evaluated by local relapse rate, Tolerance of interstitial brachytherapy of the anal canal evaluated by the rate of chronic toxicities.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients treated by brachytherapy anal canal to boost.

排除标准

  • Patients below age of 18 years

结局指标

主要结局

Evaluation of the efficacy of interstitial brachytherapy of the anal canal

时间窗: 1 year

Efficacy of anal canal interstitial brachytherapy evaluated by local relapse rate

Evaluation of the tolerance of interstitial brachytherapy of the anal canal

时间窗: 1 year

Tolerance of interstitial brachytherapy of the anal canal evaluated by the rate of chronic toxicities.

次要结局

  • Estimation of local control(1 year)
  • Estimation of disease free survival(1 year)
  • Estimation of overall survival(1 year)
  • Comparison of the incidence of toxicities (CTCAE v4) between the 2 groups(1 year)

研究者

发起方
Institut Paoli-Calmettes
申办方类型
Other
责任方
Sponsor

研究点 (1)

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