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NCT05431530Recruiting

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

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

Source: ClinicalTrials.gov · Last updated 27 Jun 2023 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Observational
Enrollment
108 (estimated)
First submitted
19 Jun 2022
Start date
22 Jun 2022
Primary completion date
31 May 2027
Lead sponsor
Seoul National University Hospital
NCT number
NCT05431530

What you commit to

  • Study type: Observational
  • Planned participants: 108
  • From 22 Jun 2022 to the primary completion date, 31 May 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patient who underwent low anterior resection in the past
  • Patient who underwent radiation therapy to abdominal or pelvic cavity

Other illness

  • Past history of gastrointestinal malignant tumor except to ovarian cancer
  • Patient who have intellectual disability or dementia

Other

  • Patient who have colostomy
  • ECOG performance status over 3
  • Patient taking opioid analgesics

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Seoul National University Hospital
Coordinator of this site? Confirm its status
SeoulSouth KoreaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.