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Assessments of Sarcopenia Prevalence in Chronic Heart Failure Patients and in Subjects Before TAVI

Assessments of Sarcopenia Prevalence in Chronic Heart Failure Patients and in Subjects Before Transcatheter Aortic Valve Implantation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03153774
Acronym
PRESAR-HF
Enrollment
300
Registered
2017-05-15
Start date
2014-11-03
Completion date
2018-12-31
Last updated
2017-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Heart Failure, Sarcopenia

Keywords

Sarcopenia, Heart failure (HF), The trans aortic valvular implantation (TAVI)

Brief summary

The main objective was to assess the prevalence of sarcopenia in chronic heart failure patients and in patients before the trans aortic valvular implantation. The loss of muscle mass in chronic heart failure patients is a prognostic factor for sarcopenia. The purpose was to identify in these patients signs of sarcopenia for a better management.

Detailed description

Age-related muscle loss, termed sarcopenia, affects 10% of elderly subjects aged 60-70 years and more than 30% above the age of 80. The concept of sarcopenia has been supported by the recent findings of muscular atrophy which was related to the decrease of protein synthesis because of the anabolic resistance, affecting the muscular fibers type II. In fact, sarcopenia could be a consequence of chronic disease and not only an issue in the elderly people. The diagnosis is assessed by the weak muscle mass and the muscle strength and function. A description of these muscle parameters has been described in a study of 200 patients with NYHA class II-III and showed that 19,5 % have a decrease in muscle mass. They also showed that these patients have a lower functional ability. These findings prompted us to investigate the prevalence of sarcopenia in chronic heart failure subjects for a better management of these patients.

Interventions

DIAGNOSTIC_TESTAssessment of sarcopenia prevalence

Handgrip test, Bioimpedance analysis (Bodystat), 6-min walking test, Short physical performance battery (balance test, 4-min walking test, 5 times getting-up test), Biological markers test, Trans-thoracic echography, Electrocardiogram 12 leads, Palm gripping test

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Masking description

Open

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Major patients (\>18 years) * Men or women * Hospitalized in pre- trans aortic valvular implantation assessment in the cardiology department of the university hospital centre of Clermont-Ferrand or * Patients with chronic heart failure in charge in the hospital of Clermont-Ferrand or convalescence in the pneumocardiological clinic of Durtol

Exclusion criteria

* Patient not affiliated to social security * Inability to understand the information consent letter * Not having signed informed consent * Has a mental or legal incapacitation and is unable to provide informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Bioimpedance analysis dataat day 1Fat-free mass and body fat mass will be combined to report BMI in Kg/m2
Short physical performance batteryat day 1Balance test, 4-min walking test, 5 times getting-up test
Handgrip testat day 1

Secondary

MeasureTime frameDescription
complete blood count CBC (white blood cells in Giga/L and red blood cells in Tera/L)at day 1Measure of inflammation
urea in mmol/Lat day 1Measure of inflammation
albumin in g/Lat day 1Measure of inflammation
Blood draw for serum creatinine in umol/Lat day 1Measure of inflammation
Electrocardiogramat day 1Parameter which may interfere with sarcopenia
Trans-thoracic echographyat day 1Parameter which may interfere with sarcopenia
NT-ProBNP in ng/Lat day 1Measure of inflammation
CRP in mg/Lat day 1Measure of inflammation
platelets in Giga/Lat day 1Measure of inflammation

Countries

France

Contacts

Primary ContactPatrick LACARIN
placarin@chu-clermontferand.fr04 73 75 11 95
Backup ContactRomain ESCHALIER, PhD
reschalier@chu-clermontferrand.fr0033 473 751 410

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026