RecruitingNot Applicable

Post-stroke Cognitive Impairment

Switzerland600 participantsStarted 2020-12-17

Plain-language summary

Present study aims to track the post-stroke cognitive trajectories and to investigate its inter-individual variability.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age ≥18 years old * First-ever anterior circulation ischemic stroke confirmed by routine MRI * Time of enrollment: ≤ 10 days from stroke onset. Exclusion Criteria: * Previous stroke anamnestic or based on clinical imaging * Additional stroke in posterior circulation * Conditions that preclude the cognitive testing (e.g. delirium, intubation, reduced vigilance * Neurological or psychiatric conditions that preclude the data interpretation (e.g. pre-stroke dementia, schizophrenia, brain tumor, regular intake of benzodiazepine, depression) * MRI contraindication * Native language other than German, French or Italian

What they're measuring

Number of participants with delayed cognitive deterioration (DCD)

Timeframe: at 3 months, at 12 months and at 36 months post-stroke

Number of participants with delayed functional deterioration

Timeframe: at 3 months, at 12 months and at 36 months post-stroke

Trial details

NCT IDNCT05653141

SponsorRoza Umarova

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2026-10-31

Contact for this trial

Roza M. Umarova, PD Dr.

+41316327000 roza.umarova@insel.ch

View on ClinicalTrials.gov More First-ever Ischemic Stroke trials