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Clinical Trials in France / NCT06880432
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Sarcopenic Obesity: Estimation of Prevalence and Identification of Clinical and Biological Determinants in a Cohort of Adult Obese Patients and Longitudinal Follow-up

NCT06880432 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2025-03
Last updated
2025-03-17

Condition(s) studied

Obesity and Overweight

Investigational drug(s) / intervention(s)

Collection of fluid samples

Collection of fluid samples: \- Blood sampling, urine sampling and tissue sampling

Study summary

Context: Obesity, defined as excessive body fat, can lead to disability and loss of autonomy. If there is concomitant quantitative and qualitative muscle loss, sarcopenic obesity (SO) is suspected in this context. Although this clinical entity was defined several years ago, it is only very recently that precise assessment criteria have been established for screening and diagnosing this pathology (Donini et al. 2022).

Defined by the ESPEN/EASO consensus, SO has various consequences for health, particularly in terms of mobility and worsening of co-morbidities. It is therefore necessary to screen for SO, to determine its prevalence in the general population and to identify the determining factors in the loss of muscle mass during obesity. Most studies on the prevalence of sarcopenic obesity focus on the elderly population, bearing in mind that the prevalence of this syndrome in the elderly will increase rapidly as a result of the shift in the incidence of obesity from adults to this population in the coming decades.

The aim of this project is to determine the prevalence and determining or predisposing factors for sarcopenic obesity in a population of obese people in a broad age range (18-70 years).

Longitudinal follow-up of this cohort is planned in order to assess multifactorial changes (body composition, muscle function and physical performance) at 5 and 10 years after their inclusion in the OBESAR-2 study. In addition, patients who have undergone bariatric surgery will also be followed in the shorter term to analyse the phenotypic changes induced by rapid weight loss on muscle loss.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Age: 18-70 * Sex: men and women * Clinical nutrition patient receiving a metabolic assessment to optimise clinical and paraclinical management * Patient meeting obesity criteria defined by BMI \> 30 kg/m². * Patient of legal age who has given free, informed and signed consent * Patient covered by social security Non-inclusion criteria : * Patients with cancer or severe chronic disease (renal failure, respiratory failure, liver failure) * Patients with neuromuscular disease * Patient with total walking disability * Patients who are minors * Patient refusing to take part in the study * Pregnant or breast-feeding women * Under guardianship, curatorship, deprived of liberty or under court protection * Patient who has taken part in the OBESAR study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHU Clermont-Ferrand Clermont-Ferrand France

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06880432 on ClinicalTrials.gov ↗ ← All trials in France