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Clinical Trial Summary

This study aims to evaluate the relationship between sarcopenia and functional outcomes with temporal muscle mass change.


Clinical Trial Description

It is well known that stroke increases the risk of developing sarcopenia . In addition, prestroke sarcopenia is associated with worse functional outcomes in patients with stroke. Temporal muscle thickness (TMT) has recently been proposed as a new marker of whole-body muscle mass and function. Measurement of temporal muscle mass by computed tomography (CT) and magnetic resonance imaging (MRI) has been studied in the literature in recent years. All stroke patients undergo cranial CT or MRI examinations at the time of admission. By evaluating the temporal muscle mass of these patients with these examinations, information about pre-stroke muscle mass and sarcopenia can be obtained. Ultrasonography (USG), on the other hand, may be a more accessible, less expensive, and safer option for assessing muscle mass in the follow-up of stroke patients. This study aims to evaluate the relationship between sarcopenia and functional outcomes with temporal muscle mass change by MRI/CT at admission and by USG in the chronic period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05456646
Study type Observational
Source Bozyaka Training and Research Hospital
Contact
Status Enrolling by invitation
Phase
Start date July 15, 2022
Completion date April 2024

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