跳至主要内容
临床试验/NCT04279080
NCT04279080已完成不适用

Low Anterior Resection Syndrome (LARS) in Ovarian Cancer Patients - a Multi-centre Comparative Analysis.

Medical University of Vienna0 个研究点目标入组 125 人开始时间: 2003年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
125
主要终点
functional bowel outcome after low anterior resection

研究概览

简要总结

Background:

Low anterior resection syndrome (LARS) is a common functional disorder after low anterior resection impacting quality of life. Data on LARS derives nearly exclusively from rectal cancer studies. Therefore, the study was designed to assess LARS in advanced epithelial ovarian cancer (EOC) patients, who underwent rectal resection and to compare it with a female rectal cancer cohort.

Methods:

A cross-sectional multi-centre analysis was performed for female patients suffering from either rectal or EOC who received a low anterior resection as part of their therapy regimen. None of the patients received pre- or postoperative radiotherapy. LARS was defined by using the validated LARS score and its severity was divided into "no", "minor" and "major LARS".

研究设计

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

入排标准

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

入选标准

  • low anterior resection because of ovarian or rectal cancer

排除标准

  • neoadjuvant or adjuvant radiotherapy

结局指标

主要结局

functional bowel outcome after low anterior resection

时间窗: 1 year

low anterior resection syndrome score, questionnaire via telephone call or personal contact

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Felix Harpain

Principle Investigator, M.D.

Medical University of Vienna

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