RecruitingNCT07611136

Cerebral Small Vessel Disease Progression Dependent on Stroke Type

Biomarker-based Assessment of Cerebral Small Vessel Disease Progression After Lacunar and Territorial Stroke - a Prospective Cohort Study


Sponsor

Johannes Dorst

Enrollment

180 participants

Start Date

Mar 26, 2026

Study Type

OBSERVATIONAL

Conditions

Summary

The goal of this prospective, observational study is to understand if cerebral small vessel disease (CSVD) has different velocities and patterns of temporal development, dependent on a concurrent ischemic stroke. It focusses on adult patients with known or newly diagnosed CSVD on magnetic resonance imaging. The study will evaluate if blood based, in parts central nervous system specific protein markers, so called biomarkers, have an additional value reflecting the course of CSVD as defined per MRI assessments. Further patient-relevant endpoints include neuropsychological abilities, neurological functional outcomes, quality of life assessments, stroke recurrence risk.


Eligibility

Min Age: 18 Years

Inclusion Criteria8

  • Age ≥ 18 years
  • Evidence of cerebral small vessel disease on brain MRI, defined as white matter hyperintensities (Fazekas grade 1-3)
  • Assignment to one of the following study groups based on MRI findings:
  • cerebral small vessel disease without evidence of an acute ischemic stroke
  • cerebral small vessel disease with acute lacunar ischemic stroke
  • cerebral small vessel disease with acute territorial ischemic stroke
  • Ability to provide written informed consent
  • Sufficient German language skills to understand study procedures and assessments

Exclusion Criteria7

  • Alternative plausible causes of white matter hyperintensities other than cerebral small vessel disease (e.g. inflammatory central nervous system disorders, leukodystrophies, brain tumors)
  • Known neurodegenerative diseases (e.g. Parkinson's disease, Alzheimer's disease, other dementias)
  • Acute or recent traumatic brain injury
  • Contraindications to magnetic resonance imaging
  • Pregnancy or breastfeeding
  • Life expectancy of less than one year
  • Inability to comply with study procedures or follow-up visits

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(1)

University Hospital Ulm, Department of Neurology, Germany

Ulm, Baden-Wurttemberg, Germany

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07611136


Related Trials