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Sarcopenia in Acute Ischemic Stroke

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07764172
Enrollment
400
Registered
2026-08-13
Start date
2026-08-01
Completion date
2029-12-31
Last updated
2026-08-13

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

Conditions

Acute Stroke, Sarcopenia

Keywords

sarcopenia, acute stroke

Brief summary

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.

Interventions

None listed

Sponsors

University Clinical Hospital na V.V.Vinogradov (branch of RUDN university na Patrice Lumumba)
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum

Inclusion criteria

* 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 criteria

* TIA without a visible lesion on neuroimaging; bilateral hemiparesis * Amputations or severe contractures that preclude anthropometric assessment * 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 * 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

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline in Barthel Index for Activities of Daily Living at 14 daysBaseline and 14 daysLower scores indicate increasing disability and a greater need for skilled care. Min - 0 ( \< 20 - totally dependent), max - 100 ( \> 80 - independent).
Change from Baseline in Modified Rankin scale at 90 daysBaseline and 90 daysMin - 0 (no disability), max - 6 (dead). A score of 0 is no disability, 5 is disability requiring constant care for all needs; 6 is death.

Secondary

MeasureTime frameDescription
Number of Participants with sarcopeniaBaseline
Change from Baseline in arm muscle mass at 14 and 28 days.Baseline, 14 and 28 daysMid-upper arm circumference: measured at the midpoint between the acromion and the olecranon with the arm relaxed (2 measurements) in cm. Arm muscle circumference and area are calculated using the Heymsfield formula.
Change from Baseline in calf circumference at 14 and 28 daysBaseline, 14 and 28 daysCalf circumference: measured in the seated position, with the knee at a right angle, at the widest part of the non-paretic calf, with the tape snug but without compression (2 measurements) in cm. Calf circumference below 34 cm in men and 33 cm in women is classified as reduced.
Change from Baseline in handgrip strength at 14 and 28 days.Baseline, 14 and 28 days.Handgrip dynamometry: performed in the seated position with the elbow at a right angle; three trials on the non-paretic hand, with the mean value used for analysis. Handgrip strength of the non-paretic hand below 27 kg in men and 16 kg in women is classified as reduced.
Correlations between anthropometric measures and ultrasound/CT parametersBaseline, 14, 28, and 90 days
Change from Baseline in National Institutes of Health Stroke Scale (NIHSS) at 24 hours, 7 and 14 days.Baseline, 24 hours, 7 and 14 days.Min - 0, max - 42. A higher score means a patients has more severe symptoms. Patients with a score of \<4 are highly likely to have good clinical outcomes.
Change from Baseline in Rivermead Mobility Index at 14 and 28 days.Baseline, 14 and 28 days.Min - 0, max - 15. Higher scores indicate better mobility performance. A score of 0 indicates an inability to complete any of the 15 tasks.
Mortality at 14 and 90 days14 and 90 daysMortality rate at 14 and 90 days
Hospital length of stayUp to 28 daysDays. Total number of days spent admitted to the hospital during the index hospital stay, calculated from admission date to final discharge date.
Intensive care unit length of stayUp to 28 daysDays. Total number of days spent in the intensive care unit from the time of initial ICU admission to successful transfer or discharge to a step-down unit.
Number of Participants with recurrent events within 90 daysFrom baseline to 90 days

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 14, 2026