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Prevalence of Sarcopenia in Patients Admitted to ICU and Its Progression During Hospitalization.

Prevalence of Sarcopenia in Patients Admitted to ICU and Its Progression During Hospitalization.

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07303335
Acronym
SARC-ICU
Enrollment
100
Registered
2025-12-24
Start date
2025-05-14
Completion date
2026-02-28
Last updated
2025-12-24

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

Conditions

Bio-Impedance Measurements, Body Composition Measurement, Critical Illness, Intensive Care (ICU) Myopathy, Sarcopenia, Ultrasound Evaluation

Brief summary

This is a prospective, observational study at the ICU of Hospital Mútua de Terrassa, running from May to December 2025. The primary goal is to determine the prevalence of sarcopenia in adult patients requiring more than 48 hours of mechanical ventilation. Sarcopenia is assessed using the SARC-F score, impedanciometry, and quadriceps ultrasound. Secondary aims include tracking the development of ICU-Acquired Weakness (ICU-AW) using the MRC score. All data is collected anonymously after obtaining informed consent.

Interventions

None listed

Sponsors

Hospital Mutua de Terrassa
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Older than 18 years old. * Expected duration of mechanical ventilation (MV) exceeding 48 hours.

Exclusion criteria

* Refusal to participate. * Mechanical ventilation not exceeding 48 hours. * Do-not-resuscitate (DNR) orders or limitations of therapeutic effort upon admission.

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of sarcopenia at the time of ICU admission.Baseline at admission to ICUDescribe the prevalence of sarcopenia at the time of ICU admission in patients with an expected duration of mechanical ventilation (MV) exceeding 48 hours.

Secondary

MeasureTime frameDescription
Detecting patients who develop ICU-Acquired Weakness (ICU-AW) and/or prolonged mechanical ventilation weaningFrom ICU admission to 30 days follow-upDetecting patients who develop ICU-Acquired Weakness (ICU-AW) and/or prolonged mechanical ventilation weaning, defined as failure of definitive disconnection from mechanical ventilation
Detecting the appearance of other complicationsFrom admission to 30 days follow upDetecting the appearance of other complications during admission such as: the appearance of refeeding syndrome or increased prevalence of insulin resistance.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026