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NCT06704789Toborzás még nem indult

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

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2024. nov. 26. · Több mint 12 hónapja nem frissült - kérdezd meg a helyszínt, nyitott-e még

Következő lépések

Rövid összefoglaló (regiszter, angolul)

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.

Állapot (regiszter)
Toborzás még nem indult
Vizsgálattípus
Megfigyeléses
Résztvevők száma
90 (tervezett)
Első benyújtás
2024. nov. 21.
Kezdés
2024. dec. 1.
Elsődleges befejezés
2024. dec. 1.
Fő szponzor
Pusan National University Yangsan Hospital
NCT-szám
NCT06704789

Mit vállalsz

  • Vizsgálat típusa: Megfigyeléses
  • Tervezett résztvevők: 90
  • 2024. dec. 1. és az elsődleges befejezés (2024. dec. 1.) között
  • Nincs megadott helyszín, ország nélkül
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

Ki nem vehet részt

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Korábbi kezelés

  • 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.

Más betegség

  • 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.

Egyéb

  • 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.

Kiket keres a vizsgálat

  • 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.

Életkor a regiszterben: 19 év – 80 év · Nem: nők és férfiak · Egészséges önkénteseket is fogad

A teljes feltétellista: ClinicalTrials.gov

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