New study aims to improve life after gynecologic cancer
NCT ID NCT06553612
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether a special hospital visit with a team of experts can help women who finished treatment for ovarian or endometrial cancer get more of the supportive care they need. About 268 women in remission will be split into groups: some get the extra hospital assessment and a nurse coordinator, others get standard follow-up. The goal is to see if this approach leads to better use of services like nutrition, physical therapy, or counseling, and ultimately improves quality of life.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 268 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2024
- Expected to finish
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Jun 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 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 Exclusion Criteria: * Any associated medical or psychiatric condition that could compromise the patient's ability to participate in the study * Patient with locoregional or metastatic recurrence * Patient deprived of liberty, under guardianship or curatorship * Simultaneous participation in a therapeutic clinical trial
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
13 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CHU
RECRUITINGStrasbourg, France
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CHU, Besançon
RECRUITINGBesançon, France
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CHU, Saint Etienne
NOT_YET_RECRUITINGSaint-Etienne, France
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Centre Jean Perrin
NOT_YET_RECRUITINGClermont-Ferrand, France
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Centre Léon Bérard
RECRUITINGLyon, France
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François Baclesse
RECRUITINGCaen, France
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Gustave Roussy
RECRUITINGVillejuif, France
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Hopital Diaconesses Croix Saint-Simon
RECRUITINGParis, France
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Hopital Europeen George Pompidou
NOT_YET_RECRUITINGParis, France
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Hopital privé des Côtes d'Armor
NOT_YET_RECRUITINGPlérin, France
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Hôpital COCHIN
NOT_YET_RECRUITINGParis, France
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Institut Curie
NOT_YET_RECRUITINGParis, France
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Institut Curie, St Cloud
RECRUITINGSaint-Cloud, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- A phase 1, First-in-Human (FIH), Open-Label, Dose-Escalation and dose expansion study of the peptide drug conjugate (PDC), TS-104, as a monotherapy in subjects with advanced solid tumors
- Operationalising multifactorial ovarian cancer risk assessment using the CanRisk tool versus standard practices.
- Can a new drug shrink advanced solid tumors?
- Can ultrasound sharpen the surgical map for ovarian cancer near the liver?
- Can a new drug shrink tumors that resist standard care?
- Can protein patterns in stored tumors point to new treatment targets?