ClinicalTrials.Veeva

Menu

LARS in Ovarian Cancer Patients

Medical University of Vienna logo

Medical University of Vienna

Status

Completed

Conditions

Low Anterior Resection Syndrome

Treatments

Other: low anterior resection syndrome evaluation

Study type

Observational

Funder types

Other

Identifiers

NCT04279080
1201/2018

Details and patient eligibility

About

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".

Enrollment

125 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • low anterior resection because of ovarian or rectal cancer

Exclusion criteria

  • neoadjuvant or adjuvant radiotherapy

Trial design

125 participants in 2 patient groups

1
Description:
rectal cancer patients
Treatment:
Other: low anterior resection syndrome evaluation
2
Description:
ovarian cancer patients
Treatment:
Other: low anterior resection syndrome evaluation

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems