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Understanding Loss of Muscle Mass and Function (SAMANTHA)

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Withdrawn

Conditions

Sarcopenia

Study type

Observational

Funder types

Other

Identifiers

NCT04004039
RECHMPL19_0272

Details and patient eligibility

About

Sarcopenia is a loss of muscle mass and function that develops during aging. But sarcopenia is also observed in several other conditions: chronic diseases, cancers, viral infections, renal / respiratory insufficiency, immobility, obesity with low physical activity. This sarcopenia is named secondary sarcopenia to distinguish it from the age-associated primary sarcopenia. During prolonged hospitalizations in intensive care, a significant loss of muscular mass and function is also observed. This acute sarcopenia or Intensive Care Unit-Acquired Weakness (ICU-AW) may persist for several months after discharge from hospital. In addition to the loss of autonomy, the reduction of muscle mass has important metabolic implications, ranging from insulin resistance to modification of myokines production. Sarcopenia greatly increases the morbidity and mortality of patients regardless of its cause. The aim of our project is to identify the molecular mechanisms implicated in sarcopenia from different origin. We will particularly focus our work on the metabolic properties, the proliferation/ differentiation and regeneration capacities of the satellite cells (adult muscle stem cells). These satellite cells will be purified from quadriceps biopsies of human volunteers recruited at CHU Montpellier. These satellite cells will also be used to test the ability of some wild aromatic plants from south of France to improve cell survival and differentiation. This will allow us to identify the molecular mechanisms involved in sarcopenia development and identify potential therapeutic molecules.

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients undergoing quadriceps muscle biopsy as part of the treatment.
  • Patient having given their agreement of conservation within the framework of the care of the biological sample (biopsy and blood sample)

Exclusion criteria

  • Subject refusing the detection of anti-HIV, anti-hepatitis C antibodies, HBS antigen
  • Subject treated with anticoagulant, beta blocker, lipid-lowering agent (statin or fibrate), anti-inflammatory, ACE inhibitors, angiotensin 2 receptor antagonist or corticosteroids, including locally.
  • Allergic subject to local anesthetics
  • History or presence of psychoactive substance abuse
  • History of recent abdominal surgery (less than 3 months)
  • Subject deprived of liberty by judicial or administrative decision
  • Major subject protected by law
  • Inability to understand the nature and purpose of the study and / or communication difficulties with the investigator

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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