Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
125 participants
OBSERVATIONAL
2003-01-01
2018-12-31
Brief Summary
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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".
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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1
rectal cancer patients
low anterior resection syndrome evaluation
evaluation of postoperative functional bowel outcome
2
ovarian cancer patients
low anterior resection syndrome evaluation
evaluation of postoperative functional bowel outcome
Interventions
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low anterior resection syndrome evaluation
evaluation of postoperative functional bowel outcome
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
100 Years
ALL
No
Sponsors
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Medical University of Vienna
OTHER
Responsible Party
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Felix Harpain
Principle Investigator, M.D.
Other Identifiers
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1201/2018
Identifier Type: -
Identifier Source: org_study_id
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