跳至主要内容
临床试验/NCT02998619
NCT02998619已完成不适用

Retrospektive Analyse Der Radiotherapie Des Pelvinen Lymphabflusses Beim Lokalisierten Prostatakarzinom Vom Hochrisikotyp Anhand Der Klinikdatenbank 2010-2016

Kantonsspital Graubuenden1 个研究点 分布在 1 个国家目标入组 52 人开始时间: 2016年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
52
试验地点
1
主要终点
Progression-free survival

研究概览

简要总结

Men with high risk prostate cancer who underwent radiotherapy of the prostate/seminal vesicles or underwent postoperative radiotherapy including pelvic lymph nodes between 2010 and 2016 are analyzed retrospectively. The aims are to estimate progression-free survival as well as toxicity according to CTCAE v4.03.

详细描述

Collection of data and retrospective analysis of patients with high risk prostate cancer treated with radiotherapy to pelvic lymph nodes.

What influence has irradiation of pelvic lymph nodes on patients with high risk prostate cancer in terms of progression free survival and toxicity. How does this influence side effects with respect to gastrointestinal (proctitis, abdominal pain, diarrhea) and genitourinary (cystitis, urinary disorders) toxicities (CTCAE v4.03)

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Men with high risk prostate cancer treated with radiotherapy to prostate/seminal vesicles or postoperative radiotherapy and pelvic lymph nodes at the Kantonssptial Graubuenden, Department of Radiation Oncology between 2010 and 2016

排除标准

  • Men with prostate cancer other than high risk disease and no radiotherapy to pelvic lymph nodes

结局指标

主要结局

Progression-free survival

时间窗: through study completion, an average of 2 years

PSA progession-free survival will be measured

次要结局

  • Toxicity (CTCAE v4.03)(through study completion, an average of 2 years)

研究者

发起方
Kantonsspital Graubuenden
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验