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Ultrasound to Evaluate the Quadriceps Muscle Wasting

Interest of the Ultrasound to Evaluate the Quadriceps Muscle Wasting in Critical Ill Patients.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02562495
Acronym
ECHOSCAN
Enrollment
42
Registered
2015-09-29
Start date
2016-01-21
Completion date
2017-08-31
Last updated
2017-09-06

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

Conditions

Severe Cerebral Pathology

Keywords

severe cerebral pathology, Ultrasound, thickness of the quadriceps

Brief summary

Intensive care unit acquired muscle weakness (ICUAW) is a common disease. After 7 days of mechanical ventilation, a quarter of patients develop an ICUAW responsible of a 15-20% of muscle loss. This is a serious pathology associated with high morbidity and mortality. Clinical diagnosis of ICUAW is difficult and need a patient awoken. CT scan and Magnetic Resonance Imaging (MRI) are considered as gold standards to quantify and monitor changes in muscle mass. But these tools are not adapted to ICU patients. Ultrasound (US) is an easy access tool at the bedside to assess muscle mass and does not expose the patient to additional radiation. The objective of this study is to evaluate the correlation between US and CT scan to measure quadriceps muscle thickness of ICU patients.

Detailed description

As part of the monitoring of the neurological disease, brain CT scans are frequently performed. At the same time, an acquisition sequence centered on the quadriceps will follow the brain sequences. Up to three brain CT scans coupled with a quadriceps imaging will be performed between the day of admission and on the tenth day of hospitalization. An ultrasound of the quadriceps will be performed concomitantly. The thickness of the quadriceps is measured by an independent operator on CT and ultrasound images.

Interventions

DEVICECT Scan and ultrasonography

Up to three measurements (CT scan and Ultrasonography) of the thickness of quadriceps, will be made concurrently .

Sponsors

Centre Hospitalier Universitaire de Saint Etienne
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Patient over 18 years admitted to intensive care for a severe brain injury (Glasgow \<8) and with a predictive duration of mechanical of at least 48hours

Exclusion criteria

* Pregnancy, * Bilateral trauma of thighs, * Coma induced by poisoning or by a metabolic disorder, * Morbid obesity (BMI \> 35).

Design outcomes

Primary

MeasureTime frameDescription
Concordance of the measurement of the quadriceps thickness by ultrasound and by CT scanBetween the day of admission (D1) in intensive care unit and the tenth day ( D10 )Concordance of each of the three measurements of the thickness of quadriceps realised concurrently by CT scan and Ultrasonography (composite measure)

Secondary

MeasureTime frameDescription
kinetic of the thickness of quadricepsBetween the day of admission (D1) in intensive care unit and the tenth day ( D10 )Evolution of he thickness of quadriceps measure concurrently by CT scan and Ultrasonography

Countries

France

Outcome results

None listed

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