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Taking people in RussiaNo phase

Muscle loss in people hospitalized with an ischemic stroke and how they recover

Examines sarcopenia in adults with acute ischemic stroke and their recovery afterward.

Plain-language title generated from the registry record
Registry title: Sarcopenia in Acute Ischemic Stroke

Key facts

Where
Moscow, RussiaSee the site

Where in Russia

  • Moscow State Budgetary Healthcare Institution "Moscow City Hospital named after S.S. Yudin, Moscow Healthcare Department"Moscow, RussiaTaking people

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Trial details

Who runs it
University Clinical Hospital na V.V.Vinogradov (branch of RUDN university na Patrice Lumumba)
Trial code
NCT07764172
Record updated
22 October 2026
Original description
The objective of this observational study is to determine the prevalence of sarcopenia in patients aged 50 years and older with acute ischemic stroke, to characterize its trajectory during the acute phase using instrumental verification and functional-cognitive assessments, and to evaluate its impact on functional outcome at three months. The main research question is:Read full original descriptionShow less

Sarcopenia in Patients During the Acute Phase of Ischemic Stroke: Multimodal Assessment and Three-Month Functional Outcomes

The objective of this observational study is to determine the prevalence of sarcopenia in patients aged 50 years and older with acute ischemic stroke, to characterize its trajectory during the acute phase using instrumental verification and functional-cognitive assessments, and to evaluate its impact on functional outcome at three months. The main research question is:

Is the presence of sarcopenia at admission associated with less favorable stroke outcomes, including higher rates of complications and mortality?

Participants receiving standard medical care for acute ischemic stroke will undergo extended functional assessment for sarcopenia, and a subset will additionally undergo cognitive evaluation.

Inclusion: Age 50 years and older; Acute ischemic stroke confirmed by CT or MRI; Admission within the first 72 hours; Written informed consent and availability of a contact telephone number for follow-up.

Exclusion: Active cancer at stage IV or life expectancy of less than 3 months; Neuromuscular diseases; chronic use of systemic glucocorticoids for more than 3 months; TIA without a visible lesion on neuroimaging; bilateral hemiparesis; Amputations or severe contractures that preclude anthropometric assessment; Pregnancy; refusal to participate; Discontinuation criteria (drop-out); Discharge or death within the first 7 days; Withdrawal of consent; Transfer to another facility resulting in loss of contact.

ClinicalTrials.gov NCT07764172