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NCT05415527Completed

Evaluation of Pretreatment Sarcopenia in Patients With Inoperable High-grade Ovarian Carcinoma as Part of Optimised Management

Source: ClinicalTrials.gov · Last updated 13 Oct 2026

Brief summary (registry, in English)

Prospective, monocentric study evaluating the presence of sarcopenia prior to neoadjuvant chemotherapy and during chemotherapy as part of optimised management.

Status (registry)
Completed
Study type
Interventional
Enrollment
25 (actual)
First submitted
7 Jun 2022
Start date
11 Jun 2022
Primary completion date
30 Apr 2025
Lead sponsor
Institut Bergonié
NCT number
NCT05415527

What you commit to

  • Study type: Interventional
  • Participants enrolled: 25
  • From 11 Jun 2022 to the primary completion date, 30 Apr 2025
  • 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.

Age

  • Patients over the age of 70 the G8 of whom requires oncogeriatric surgery.

Other

  • Contraindication to CT-scans.
  • Contraindication to bone mineral densitometry.
  • Patients under guardianship, vulnerable patients or patients under any other legal protection measures.
  • Geographic, social or psychological factors meaning the patient is unable to commit to study follow-up and procedures.
  • Patient already included in this study or in another study evaluating the impact of sarcopenia.

Who the study is looking for

  • Age ≥ 18 years.
  • Inoperable, high-grade, epithelial ovarian carcinoma requiring perioperative chemotherapy (neoadjuvant and adjuvant).
  • Optical medical treatment (carboplatin-taxol chemotherapy every 3 weeks) and surgery at Institut Bergonié.
  • Non-clinically undernourished patient, i.e. without loss of more than 10% bodyweight in 6 months
  • Free, informed and written consent signed by the participant and the investigator (on the day of inclusion at the latest and before any tests required for the research).
  • Patient with social security cover in accordance with Article 1121-11 of the French code of public health.

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
Institut Bergonie
Coordinator of this site? Confirm its status
BordeauxFranceUnknown status

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