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Neuronal correlates of post-stroke epilepsy and the associated cognitive impairment

Neuronal correlates of post-stroke epilepsy and the associated cognitive impairment - PoSECI-7T

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON46873
Enrollment
72
Registered
2017-06-21
Start date
2018-09-21
Completion date
Unknown
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

epilepsy after brain infarction post-stroke epilepsy

Interventions

None listed

Sponsors

Medisch Universitair Ziekenhuis Maastricht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Patients suffering from stroke (and post-stroke epilepsy), including both brain infarction, cerebral hemorrhage and clinically significant hemorrhagic transformation of stroke (or a primary intracerebral hemorrhage) - Patients suffering from post-stroke epilepsy after cortical stroke defined as one or more unprovoked epileptic seizures occurring more than one week after the stroke, according to International League Against Epilepsy criteria. - Patients suffering from cortical stroke, with the onset of acute stroke symptoms more than 4 months prior to inclusion. - Age > 18 years

Exclusion criteria

Exclusion criteria: -onset of stroke (and epilepsy for post-stroke epilepsy patients) less than 4 months ago -In case of the PSE group: onset of epilepsy within a week or 2 years after the onset of stroke. -previous history of epilepsy -history of another cerebral disorder (neurodegenerative diseases, tumours) -inability to provide informed consent - any contraindication for MRI: metallic foreign body, pacemaker, claustrophobia, pregnancy, tattoos, permanent make-up. - known contrast allergy to gadolinium, insufficient kidney function (eGFR

Design outcomes

Secondary

MeasureTime frame
- Stroke and post-stroke epilepsy outcome will be assessed using the NIHSS. - All patients and healthy controls will undergo cognitive testing: • To assess level of function Raven's Progressive Matrices is used. • To assess central processing speed the CVST will be used. • In addition the highest premorbid educational level will be determined. Laesional deficits (such as dysphasia) will be tested at inclusion.

Primary

MeasureTime frame
- BBB permeability as determined by DCE-MRI to assess the leakiness of the cerebral vasculature by dynamically measuring the rate of contrast agent transfer from blood into the interstitial space (leakage rate; units: mL / (min 100 g tissue)). We will compare BBB permeability in PSE patients with non-PSE patients and healthy controls. - Perfusion as determined by DSC MRI. With this method we obtain information about the CBF, the cerebral blood volume (CBV), and mean transit time (MTT). We will compare these in PSE patients with non-PSE patients and healthy controls. - Resting state functional MRI: connectivity measures, locally as well as whole brain network analysis (using graph theoretical measures) as well as DTI connectivity measures, locally (mean diffusivity/fractional anisotropy) and anatomical features (measured by standard T2, SWI and FLAIR sequences: gliosis, iron deposits microbleeds, dilated perivascular spaces, and cortical and subcortical ischemic lesions).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)