Clinical trial Recruiting at 1 site Observational Ages 18 and up Women only

Evaluating quality of life after surgery for advanced ovarian cancer

Official title: Assessment of Quality of Life After Low Anterior Resection or Visceral Peritoneal Stripping During cytOreDuctive surgerY for Advanced Ovarian Cancer Requiring Tumor Resection on the Rectosigmoid Colon: a Prospective Cohort Study

Run by Seoul National University Hospital · NCT05431530 · Data updated 2026-11-12

This study looks at how surgery for advanced ovarian cancer affects the quality of life and bowel function in patients after their operation.

More Ovarian Cancer trials

Quick facts

Study typeObservational
Ages18 Years and up
SexWomen only
Enrollment108 (estimated)
SponsorSeoul National University Hospital
Academic / other
Drugs / interventionschemotherapy, radiation
Locations1 site (Seoul)
StatusRecruiting
StartedJune 22, 2022
Main results expectedMay 31, 2027
Study endsMay 31, 2027
Registry record updatedJune 27, 2023
Trial IDNCT05431530 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults over 18 with newly diagnosed ovarian cancer or related conditions who are scheduled for cytoreductive surgery.

Probably not a fit

Patients who have previously undergone low anterior resection or have other significant gastrointestinal issues may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study assesses the incidence of low anterior resection syndrome and the overall quality of life in patients who have undergone cytoreductive surgery for advanced ovarian cancer. It focuses on individuals who require the removal of tumors from the rectum and sigmoid colon, which can lead to complications affecting bowel function. By monitoring these patients post-surgery, the study aims to gather data on their recovery and the challenges they face related to bowel control and daily living. The findings could provide valuable insights into patient care and management following such surgical interventions.

Why it matters

Potential benefit: If successful, this study could improve understanding of post-surgical quality of life and lead to better management strategies for patients with advanced ovarian cancer.

How similar studies have gone: While there have been studies on quality of life post-surgery for various cancers, this specific focus on low anterior resection syndrome in ovarian cancer is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 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

Exclusion Criteria:

* 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
* ECOG performance status over 3
* Patient taking opioid analgesics
* Patient who have intellectual disability or dementia

Where it's running

  • Seoul National University Hospital
    Seoul, South Korea
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.