Prospective Study of Detection of Sarcopenia in Clinical Practice for Patient With Ovarian or Endometrial Cancer

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorCentre Hospitalier Metropole Savoie

About this trial

Prospective monocentric study, non-randomized of the detection of sarcopenia in clinical practice in patients with ovarian or endometrial cancer requiring systemic oncological treatment.

main question : Identify the criteria correlated with the presence of sarcopenia (defined by the measurement of the IMS by the CT-X method in L3) among the impedancemetry and the HAS malnutrition criteria.

Data collection will be done at 6 months, 12 months after the date of inclusion.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients at least 18 years old

Patient presenting with a diagnosis of cancer of ovarian origin with an indication for chemotherapy

Patient with a diagnosis of endometrial cancer with an indication for chemotherapy

Patient with no diagnosis of other types of cancer in the previous five years

Disqualifiers

Patient with cancer of ovarian origin not requiring chemotherapy treatment

Patient with endometrial cancer not requiring chemotherapy treatment

Discovery of an intercurrent cancer other than skin or cervix cancers.

Patient wearing a Pace maker

Trial design

Design model

Single group

Treatments tested in this trial

  • Sarcopenia diagnostic test

    Diagnostic test

    measurement of impedance and physical tests ("hand grip" dynamometer, walking test), SEFI nutritional intake questionnaire

Treatment groups

75 Participants
are divided into 1 treatment group
Group A: InterventionnalExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

clinical screening for sarcopenia

Identify the criteria correlated with the presence of sarcopenia (defined by the measurement of the IMS by the CT-X method in L3) among the impedancemetry and the HAS malnutrition criteria.

Time frame
36 month
2

Proposal of a composite score for the detection of sarcopenia usable in clinical routine

Statistical analysis of sarcopenia and undernutrition data

Time frame
36 month

Secondary outcomes

Other outcomes

Sponsors and contacts

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