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RECRUITINGOBSERVATIONAL

The Role of Circadian Factors in Regulation of Neuroplasticity in Ischemic Stroke (Observational)

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The study is aimed at the investigation of the association of biomarkers of circadian rhythms with sleep characteristics and stroke outcome in acute stroke patients. It is designed as an observational cohort study with the retrospective and prospective longitudinal arms.

Who May Be Eligible (Plain English)

Who May Qualify: - acute (symptom onset to admission \<1 days) ischemic stroke - ischemic stroke affecting the branches of anterior cerebral artery, middle cerebral artery and posterior cerebral artery - age 18-80 years - moderate or severe stroke (National Institutes of Health Stroke Scale, NIHSS\>=5) - intravascular stroke treatment with thrombolysis or thrombectomy leading to satisfactory reperfusion (if applicable) - willing to sign a consent form Who Should NOT Join This Trial: - secondary parenchymal hemorrhage (\>hemorrhage index -2) - clinically unstable or life-threatening conditions - known progressive neurological diseases - known psychiatric diseases - concomitant benzodiazepine medication - drug or alcohol abuse - pregnancy - disability to participate in the study - congestive heart failure with reduced ejection fraction (\<=45%) or New York Heart Association (NYHA) classification III-IV functional class Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * acute (symptom onset to admission \<1 days) ischemic stroke * ischemic stroke affecting the branches of anterior cerebral artery, middle cerebral artery and posterior cerebral artery * age 18-80 years * moderate or severe stroke (National Institutes of Health Stroke Scale, NIHSS\>=5) * intravascular stroke treatment with thrombolysis or thrombectomy leading to satisfactory reperfusion (if applicable) * informed consent Exclusion Criteria: * secondary parenchymal hemorrhage (\>hemorrhage index -2) * clinically unstable or life-threatening conditions * known progressive neurological diseases * known psychiatric diseases * concomitant benzodiazepine medication * drug or alcohol abuse * pregnancy * disability to participate in the study * congestive heart failure with reduced ejection fraction (\<=45%) or New York Heart Association (NYHA) classification III-IV functional class

Treatments Being Tested

OTHER

No intervention is planned

No intervention is planned

Locations (1)

Almazov National Medical Research Centre
Saint Petersburg, Russia