Assessment of Quality of Life After Low Anterior Resection During Cytoreductive Surgery for Advanced Ovarian Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorSeoul National University Hospital

About this trial

This study aims to evaluate the incidence of low anterior resection syndrome and quality of life after cytoreductive surgery for advanced ovarian cancer patients.

Eligibility criteria

Qualifiers

Those with newly diagnosed ovarian cancer, fallopian tube cancer and primary peritoneal carcinomatosis who plan to undergo cytoreductive surgery and secondary cytoreductive surgery after neoadjuvant chemotherapy.

Patients with PCDS or rectal and sigmoid coloni tumor invasion suspected on the preoperative image and need resection of the tumor and clinical FIGO stage IIIB or higher

ECOG performance status : 0-2

Age over 18

Disqualifiers

Patient who underwent low anterior resection in the past

Past history of gastrointestinal malignant tumor except to ovarian cancer

Patient who have colostomy

Patient who underwent radiation therapy to abdominal or pelvic cavity

Trial design

Treatments tested in this trial

  • Cytoreductive surgery

Treatment groups

108 Participants
are divided into 1 treatment group