Fact CheckerSign in

NCT06553612Recruiting

Impact of a Multidisciplinary Assessment in Day Hospitalization Versus Standard Care on the Deployment of Supportive Oncology Care Recommended by the Personalized Post-cancer Plan in Patients at the End of Initial Treatment for Gynecological Ovarian and Endometrial Cancer Endometrial Cancer

Source: ClinicalTrials.gov · Last updated 24 Sept 2026

Brief summary (registry, in English)

This project proposes a structuring of supportive oncology care for the recovery phase after gynecological cancer (ovarian/trope/peritoneum or endometrium). Patients will be divided into three groups based on the identification of oncological support care needs. Patients with supportive oncology care needs will be randomized into two groups: the experimental group, receiving a personalized post-cancer plan with a multidisciplinary assessment of supportive oncology care needs in a day hospital and coordinated follow-up by the referring study nurse, and the control group, receiving a personalized post-cancer plan without a day hospital. Randomization will be stratified according to tumor location (ovary vs. endometrium), use of supportive oncology care during treatment, and treatment center. Patients with no need for supportive oncology care will be followed in an observational cohort. The main objective is to identify and manage the supportive oncology care needs of patients in remission from endometrial or ovarian cancer to improve their quality of life and post-treatment follow-up. A medico-economic analysis will be performed.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
268 (estimated)
First submitted
12 Aug 2024
Start date
7 Jun 2024
Primary completion date
7 Sept 2028
Lead sponsor
Centre Francois Baclesse
NCT number
NCT06553612

What you commit to

  • Study type: Interventional
  • Planned participants: 268
  • From 7 Jun 2024 to the primary completion date, 7 Sept 2028
  • 13 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.

Other illness

  • Any associated medical or psychiatric condition that could compromise the patient's ability to participate in the study

Other

  • Patient with locoregional or metastatic recurrence
  • Patient deprived of liberty, under guardianship or curatorship
  • Simultaneous participation in a therapeutic clinical trial

Who the study is looking for

  • Patient \> 18 years
  • Patients in remission from first-line treatment of endometrial or ovarian/tumor/peritoneal cancer.
  • Patient who has completed her initial treatment; patients on maintenance therapy are eligible.
  • Fluency in French
  • Patient with access to a telephone line
  • Patient affiliated to a social security scheme
  • Signature of informed consent prior to any specific study procedure

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

Full criteria on ClinicalTrials.gov

Sites (13)

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

SiteCityCountrySite status
CHU Besançon
Coordinator of this site? Confirm its status
BesançonFranceRecruiting
François Baclesse
Coordinator of this site? Confirm its status
CaenFranceRecruiting
Centre Jean Perrin
Coordinator of this site? Confirm its status
Clermont-FerrandFranceNot yet recruiting
Centre Leon Berard
Coordinator of this site? Confirm its status
LyonFranceRecruiting
Institut Curie
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
Hopital Européen George Pompidou
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
Hopital Diaconesses-Croix Saint Simon
Coordinator of this site? Confirm its status
ParisFranceRecruiting
Hôpital Cochin
Coordinator of this site? Confirm its status
ParisFranceNot yet recruiting
Hôpital Privé des Côtes d'Armor
Coordinator of this site? Confirm its status
PlérinFranceNot yet recruiting
Institut Curie, St Cloud
Coordinator of this site? Confirm its status
Saint-CloudFranceRecruiting
CHU Saint-Etienne
Coordinator of this site? Confirm its status
Saint-EtienneFranceNot yet recruiting
CHU
Coordinator of this site? Confirm its status
StrasbourgFranceRecruiting
Gustave Roussy
Coordinator of this site? Confirm its status
VillejuifFranceRecruiting

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