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Recruiting NCT05878002

"Cognitive, Motor and Sleep Evaluation in Patients With Ischemic Stroke of Basal Ganglia After Thrombectomy"

No phase Interventional Post-stroke Disorders

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: polysomnography.
Who it may be relevant to
Registry conditions: Post-stroke Disorders. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The goal of this interventional study is to learn about the clinical outcomes of acute ischemic stroke treated with mechanical thrombectomy resulting in a selective ischemia of the basal ganglia. The main question it aims to answer is: • defining the prevalence and clinical features of possible cognitive, motor and sleep disfuncions occuring after acute ischemic stroke treated with thrombectomy Participants will be tested for cognitive, movement and sleep disorders in the acute phase and successively in the long term follow-up.

Interventions

  • Device polysomnography
    Sleep study through polysomnographic examination

Primary outcome measures

  • Post-stroke cognitive dysfunction [Time frame: Within 72 hours]

Eligibility criteria

Inclusion criteria

  • participant's age ≥ 18 years
  • acute ischemic stroke due to occlusion of proximal middle cerebral artery successfully treated with mechanical thrombectomy (mTICI ≥ 2B)
  • signature of specific written informed consent

Exclusion criteria

  • unstable clinical conditions
  • personal history of cognitive decline before the acute ischemic stroke

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

Italy · 1 center
  • Flavia Torlizzi — Rome

Identifiers

NCT: NCT05878002 · 5137

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗