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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06320158
Other study ID # PNRR-MAD-2022-12376672
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 22, 2023
Est. completion date December 31, 2024

Study information

Verified date March 2024
Source IRCCS San Raffaele
Contact Patrizia Rovere Querini, PhD, MD
Phone +390226436095
Email rovere.patrizia@hsr.it
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Ageing is characterised by a change in body composition with a parallel decrease in muscle mass and an increase and central redistribution of fat. When drastically exacerbated, these two processes culminate in a condition known as sarcopenic obesity (SO). SO is characterised by the coexistence of obesity and sarcopenia (i.e. reduced muscle mass and function) and is a growing public health problem in the elderly. The health risks of obesity and sarcopenia act synergistically, maximising the risk of disability of OS. The molecular mechanisms underlying OS are largely unknown. Increased fat mass induces chronic systemic inflammation and alters the profiles of adipokines and hormones, promoting the development of sarcopenia. On the other hand, the reduction in muscle tissue (SM) typical of sarcopenia is characterised by an alteration in the metabolic properties of skeletal muscle with an increase in insulin resistance and a reduction in energy expenditure that favours the accumulation and dysfunction of adipose tissue (AT). The cellular alterations that would seem to underlie OS are: altered autophagy, cellular senescence, epigenetic and mitochondrial alterations and maladaptive activation of intra- and intercellular inflammatory circuits (e.g. cytokines, extracellular vesicles, dysfunctional circulating leukocytes). However, the interconnections between these mechanisms are still unclear. The impact of OS can be dramatic on the health and quality of life of those affected. Therefore, the identification of early biomarkers that can recognise overweight and obese individuals at risk of developing SO is of paramount importance. This would shed light on the heterogeneity of an otherwise homogeneous clinical condition, opening new horizons towards the conscious design of more personalised therapeutic strategies, allowing a more rational use of the limited resources available for the growing elderly population. The study design designed to achieve this aim is a cross-sectional observational study with an additional multicentre procedure lasting two years.


Recruitment information / eligibility

Status Recruiting
Enrollment 1108
Est. completion date December 31, 2024
Est. primary completion date October 31, 2024
Accepts healthy volunteers
Gender All
Age group 65 Years to 99 Years
Eligibility Inclusion Criteria: patients who are candidates for hip surgery - patients who are candidates for hip surgery - age = 65 years - patients able to give consent healthy subjects - healthy subjects from the geriatric cohort studied in 2016-2017 who at that time were: were overweight (25 = BMI < 30 kg/m2) or obese (BMI = 30 kg/m2) but had not yet developed sarcopenia Exclusion Criteria: All partecipants - unavailability to participate in the study - inflammatory or neurological myopathies - acute heart failure - active cancer

Study Design


Related Conditions & MeSH terms


Intervention

Other:
clinical evaluation of sarcopenic obesity
completion of scales and questionnaires, venous blood sampling, muscle ultrasound scan

Locations

Country Name City State
Italy Ospedale San Raffaele Milan

Sponsors (1)

Lead Sponsor Collaborator
IRCCS San Raffaele

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Identifying new molecular markers in elderly patients with sarcopenic obesity Identifying new molecular markers in elderly patients with sarcopenic obesity May 2023- October 2024
Secondary Assessing the ability of new markers (identified in the pre-clinical phase of this project) to predict individual disease trajectories Assessing the ability of new markers (identified in the pre-clinical phase of this project) to predict individual disease trajectories May 2023- October 2024
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