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NCT06704789Not yet recruiting

Investigation of the Possibility of Determining Cerebrovascular Disease Based on Hemodynamic Information of Localized Brain Regions

Source: ClinicalTrials.gov · Last updated 26 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The purpose of this study is to compare hemodynamic information from localized brain regions between stroke patients and healthy adults using brain activity data (fNIRS and EEG) and to assess the accuracy of early stroke diagnosis and classification predictions.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
90 (estimated)
First submitted
21 Nov 2024
Start date
1 Dec 2024
Primary completion date
1 Dec 2024
Lead sponsor
Pusan National University Yangsan Hospital
Diseases
Stroke
NCT number
NCT06704789

What you commit to

  • Study type: Observational
  • Planned participants: 90
  • From 1 Dec 2024 to the primary completion date, 1 Dec 2024
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of medications that could influence brain hemodynamics (e.g., antihypertensives, anticoagulants, antiplatelets, or antidepressants).
  • Participation in a study and use of experimental drugs within the past 30 days.
  • Major surgery in the past 6 months.

Other illness

  • History of head trauma in the past 6 months.
  • Ongoing severe chronic diseases (e.g., heart failure, chronic kidney disease, chronic lung disease).
  • Severe psychiatric disorders such as schizophrenia, major depression, or bipolar disorder.
  • Acute infections or inflammatory diseases.
  • Cognitive impairment or dementia.
  • Neurological disorders.

Other

  • Pregnant or breastfeeding women.
  • Inability to understand the study procedures or unwillingness to provide voluntary consent.
  • Any other clinical concerns deemed inappropriate for participation by the principal investigator or study team.

Who the study is looking for

  • For Hemorrhagic Stroke Patients :
    • Adults aged between 19 and 80 years.
    • Diagnosed with hemorrhagic stroke through clinical observation and neuroimaging.
    • First-time hemorrhagic stroke patients.
    • Hemorrhagic stroke onset between 2 weeks and 12 months prior to screening.
    • Hemorrhagic lesion located in the cortex or subcortex.
    • Not taking medications that could affect brain hemodynamics, such as - antihypertensives, anticoagulants, antiplatelets, or antidepressants.
    • Able to read and understand the informed consent form and participate in questionnaires with sufficient language proficiency.
    • Voluntarily agree to participate in the study and provide written consent, with the ability to complete the study duration.
  • For Ischemic Stroke Patients :
    • Adults aged between 19 and 80 years.
    • Diagnosed with ischemic stroke through clinical observation and neuroimaging.
    • First-time ischemic stroke patients.
    • Ischemic stroke onset between 2 weeks and 12 months prior to screening.
    • Ischemic lesion located in the cortex or subcortex.
    • Not taking medications that could affect brain hemodynamics, such as antihypertensives, anticoagulants, antiplatelets, or antidepressants.
    • Able to read and understand the informed consent form and participate in questionnaires with sufficient language proficiency.
    • Voluntarily agree to participate in the study and provide written consent, with the ability to complete the study duration.
  • For Healthy Adults :
    • Adults aged between 19 and 80 years.
    • No history of stroke or transient ischemic attack (TIA).
    • No stroke risk factors such as hypertension, diabetes, or hyperlipidemia.
    • No chronic diseases (e.g., cardiovascular disease, chronic kidney disease, chronic lung disease).
    • No psychiatric conditions (e.g., depression, schizophrenia).
    • Not taking medications that could affect brain hemodynamics, such as antihypertensives, anticoagulants, antiplatelets, or antidepressants.
    • Able to read and understand the informed consent form and participate in questionnaires with sufficient language proficiency.
    • Voluntarily agree to participate in the study and provide written consent, with the ability to complete the study duration.

Age in the registry: 19 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.