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临床试验/NCT01650987
NCT01650987已完成不适用

Prospective Observational Study of Toxicities of Cervix and Corpus Uteri Carcinomas Treatment and Evaluation of Impact on Sexual Function

Centre Oscar Lambret1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2009年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
72
试验地点
1
主要终点
Toxicities including on sexual function

研究概览

简要总结

Evaluate the toxicities of cervix and corpus uteri carcinomas treatment

详细描述

Evaluate the toxicities of cervix and corpus uteri carcinomas treatment on sexual function after treatment (radiotherapy and/or surgery)

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Patients whose treatment is provided to Centre Oscar Lambret
  • With a corpus uteri adenocarcinoma, no metastatic, treated by:
  • Surgery and observation without complementary treatment
  • Or surgery and adjuvant radiotherapy
  • Or Surgery and curietherapy of vaginal dome
  • With a cervix carcinoma, stade IA2 to IIB proximal, treated by :
  • External radiochemotherapy and curietherapy
  • Or only surgery
  • Or pre-surgical curietherapy and surgery
  • Age > 18 years

排除标准

  • 未提供

结局指标

主要结局

Toxicities including on sexual function

时间窗: up to 3 years

According to Lent-Soma, NCICTC-AE v3.0, Franco-Italian Glossary

次要结局

  • Compare the various scales of toxicity(up to 3 years)
  • Study the sexual behavior modifications(up to 3 years)
  • Specify correlation modifications of sexual behavior(up to 3 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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