C56 K59
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Ovarian cancer patients who underwent resection of sigma / rectosigmoid or deep anterior rectal resection during debulking surgery (period 2011-2018) will be recruited in this study. As a "control cohort" (this group will also be interviewed using the LARS questionnaire to record LARS score): 1) Patients who have also been treated for primary ovarian cancer but who did not receive bowel surgery as part of the debulking surgery; 2) breast cancer patients (matched-pair) who had neo / adjuvant chemotherapy based on breast cancer diagnosis, and no history of abdominal surgery .
Exclusion criteria
Exclusion criteria: All patients with diverting ostomy, postoperative anastomotic leak, history of abdominal radiotherapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of the present study is to evaluate the prevalence of the low anterior resection syndrome (LARS) in patients with advanced epithelial ovarian cancer.. | — |
Secondary
| Measure | Time frame |
|---|---|
| • Comparison of the prevalence of LARS in patients with ovarian cancer with and without sigma / rectosigmoid or deep anterior rectal resection and breast cancer patients who had no abdominal / intestinal surgery. • Prevalence of minor LARS and major LARS in patients with ovarian cancer after sigma / rectosigmoid or deep anterior rectal resection. * Evaluation of risk factors for LARS | — |
Countries
Germany
Contacts
Abteilung für Gynäkologie und Gynäkologische OnkologieKliniken Essen-Mitte