Actively Recruiting

Age: 18Years +
All Genders
NCT06650436

DEliriuM in STroke: the Link Between Stroke, Delirium and Long-term Cognitive Impairment

Led by Universitair Ziekenhuis Brussel · Updated on 2024-10-21

150

Participants Needed

1

Research Sites

105 weeks

Total Duration

On this page

Sponsors

U

Universitair Ziekenhuis Brussel

Lead Sponsor

V

Vrije Universiteit Brussel

Collaborating Sponsor

AI-Summary

What this Trial Is About

Primary objective of this study: determine whether PSD is a risk factor for PSCI, independent of brain frailty and premorbid cognitive functioning. Secondary objectives: 1. to investigate the role of infarct location, imaging markers of brain frailty and brain network disintegration in the development of PSD; 2. to investigate the role of persistent brain network disintegration in the development of PSCI.

CONDITIONS

Official Title

DEliriuM in STroke: the Link Between Stroke, Delirium and Long-term Cognitive Impairment

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 years or older
  • Clinical diagnosis of first-ever ischemic stroke with onset less than 72 hours at time of inclusion
  • Admitted at stroke unit of UZ Brussel
  • Ability to participate in cognitive assessments
  • Fluency in Dutch or French
  • Ability to undergo an EEG during the first 24 hours after onset of stroke symptoms
  • Ability to undergo MRI of the brain
Not Eligible

You will not qualify if you...

  • History of epilepsy
  • Pre-existing, space occupying brain lesion (except small meningeoma)
  • Pregnancy or wish to become pregnant
  • Severe language impairment or dementia impeding cognitive assessment
  • Life expectancy less than 1 year

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Universitair Ziekenhuis Brussel

Brussels, Belgium, 1090

Actively Recruiting

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Research Team

F

Fenne Vandervorst, MD

CONTACT

K

Karen Vandaele

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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