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Clinical Trial Summary

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".


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04279080
Study type Observational
Source Medical University of Vienna
Contact
Status Completed
Phase
Start date January 1, 2003
Completion date December 31, 2018

See also
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