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NCT02854215Completed

Cost Utility of Radical Surgery in Ovarian Cancer

Source: ClinicalTrials.gov · Last updated 14 Apr 2026

Brief summary (registry, in English)

The purpose of this study is to investigate the medico-economic impact of adherence to INCa (National Cancer Institute) guidelines in ovarian cancer surgery by assessment of outcome in cost per Quality Adjusted Life Years (QALY).

Status (registry)
Completed
Study type
Interventional
Enrollment
200 (actual)
First submitted
29 Jul 2016
Start date
18 Jan 2017
Primary completion date
15 Apr 2025
Lead sponsor
Institut Claudius Regaud
NCT number
NCT02854215

What you commit to

  • Study type: Interventional
  • Participants enrolled: 200
  • From 18 Jan 2017 to the primary completion date, 15 Apr 2025
  • 10 sites 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

  • 3\. Other malignancy diagnosed in the previous 5 years except skin cancer (other than melanoma).

Other illness

  • 2\. Patients with extra-abdominal disease, except for pleural effusion with positive cytology.

Other

  • 1\. Benign or borderline tumors.
  • 4\. Any psychological, familial, geographic or social situation, according to the judgment of investigator, potentially preventing the provision of informed consent or compliance to study procedure.
  • 5\. Patient who has forfeited his/her freedom by administrative or legal award or who is under guardianship.

Who the study is looking for

  • 1\. Woman with age ≥ 18 years.
  • 2\. Newly diagnosed ovarian, tubal or peritoneal malignancies.
  • 3\. Epithelial histology.
  • 4\. Stage IIIC or IVA with extrapelvic carcinomatosis according to FIGO classification 2014.
  • 5\. Patients undergoing primary surgery or neoadjuvant chemotherapy.
  • 6\. Performance Status ≤ 2.
  • 7\. Patient affiliated to a Social Health Insurance in France.
  • 8\. Patient information and informed consent form signed prior to any study specific procedures.

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

Full criteria on ClinicalTrials.gov

Sites (10)

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

SiteCityCountrySite status
Institut Bergonie
Coordinator of this site? Confirm its status
BordeauxFranceUnknown status
CHU Clermont-Ferrand
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Clermont-FerrandFranceUnknown status
Centre Jean Perrin
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Clermont-FerrandFranceUnknown status
Institut Paoli-Calmettes
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MarseilleFranceUnknown status
Institut Régional du Cancer Montpellier
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MontpellierFranceUnknown status
Institut Curie
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Centre Hospitalier Lyon Sud 1
Coordinator of this site? Confirm its status
Pierre-BéniteFranceUnknown status
Centre Hospitalier Lyon Sud 2
Coordinator of this site? Confirm its status
Pierre-BéniteFranceUnknown status
Institut Claudius Regaud
Coordinator of this site? Confirm its status
ToulouseFranceUnknown status
Hopital Nord Ouest Villefranche sur Saone
Coordinator of this site? Confirm its status
Villefranche-sur-SaôneFranceUnknown status

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