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Study identifier: NCT07074028 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Characterization and Longitudinal Monitoring of Muscular Phenotype in Patients Admitted to Intensive Care for Sepsis

Condition: Sepsis · Myopathy Critical Illness  ·  Sponsor: Centre Hospitalier de Saint-Brieuc

PhaseNA
Planned participants63
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Approximately 40% of patients develop muscle dysfunction during their stay in intensive care, particularly in the context of sepsis. This dysfunction represents an acquired muscle injury that is secondary to the primary illness that led to ICU admission. It affects both the limb muscles and the respiratory muscles of the thoracic cage. Clinically, this manifests as bilateral and symmetrical muscle weakness in the limbs, and contributes significantly to difficulties in weaning patients off mechanical ventilation. The loss of muscle mass is directly correlated with the severity of the patient's clinical condition and can reach up to 20% of initial muscle mass within just ten days. This rapid and profound atrophy primarily results from an imbalance between increased muscle protein breakdown (catabolism) and insufficient protein synthesis (anabolism). The consequences of this muscle dysfunction are significant and far-reaching, with a marked negative impact on the overall prognosis. This condition is associated with longer durations of mechanical ventilation and extended stays in the intensive care unit. Beyond the acute phase, patients often experience persistent reductions in physical performance, leading to long-term functional limitations that impair quality of life. Furthermore, ICU-acquired muscle dysfunction has been linked to increased long-term mortality, with excess deaths reported at both one year and five years following ICU discharge. This risk is especially pronou…

This description comes directly from the study's public registry record.

Talk to the study team

Nicolas BARBAROT  ·  +33(0)296017123  ·  nicolas.barbarot@armorsante.bzh

Frédéric DERBRE  ·  +33(0)290091588  ·  frederic.derbre@univ-rennes2.fr

Always discuss trial participation with your own doctor first.

Locations (1)

Centre Hospitalier de Saint-Brieuc - Paimpol - TréguierSaint-Brieuc, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT07074028