Effect of Sarcopenia on the Occurrence of Toxicity Related to Anti-cancer Treatments. Prospective Cohort Study

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn about the effect of sarcopenic status on the occurrence of treatment-related toxicity during the first course of anti-cancer treatment in several types of cancers. The main question it aims to answer is : Is sarcopenia a predictive marker for the occurrence of toxicity in the initial phase of cancer treatment? The evaluation will focus on the body composition of the participants, assessed by impedancemetry, and on their muscular performance by standardized physical tests.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients over 18 years old

• Patient with a diagnosis of a histologically proven solid malignant tumor with an indication for systemic treatment during initial treatment.

• CT/PET performed within 45 days before initiation of systemic treatment.

• Patient able to sign informed consent for participation in the study

• Patient affiliated to a social security system

Locations
Other Locations
France
Centre Hospitalier Metropole Savoie
RECRUITING
Chambéry
Contact Information
Primary
Aurelie FILLON
aurelie.fillon@ch-metropole-savoie.fr
04.79.96.58.13
Backup
Nathalie MARQUES, Dr
nathalie.marques@ch-metropole-savoie.fr
04.79.96.58.13
Time Frame
Start Date: 2024-06-24
Estimated Completion Date: 2028-05-01
Participants
Target number of participants: 700
Treatments
Experimental: Interventionnal
Hand Grip Dynamometer Chair rise test measurement of impedance SEFI Nutritional Intake Assessment Questionnaire GPAQ questionnaire SARC-F questionnaire
Related Therapeutic Areas
Sponsors
Leads: Centre Hospitalier Metropole Savoie
Collaborators: Université Savoie Mont Blanc

This content was sourced from clinicaltrials.gov