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Clinical Trials in Germany / NCT06128824
Active, not recruiting Observational

High Frequency Imaging in Cerebral Amyloid Angiopathy

NCT06128824 · tracked via the Priya Life Science Germany tracker
Sponsor
Martin Dichgans
Phase
Observational
Started
2019-03-19
Last updated
2025-09-12

Condition(s) studied

Cerebral Amyloid Angiopathy

Investigational drug(s) / intervention(s)

MR Imaging

MR Imaging: Serial magnetic resonance imaging (MRI)

Study summary

Cerebral amyloid angiopathy (CAA), caused by amyloid beta depositions in the walls of small cerebral vessels, is remarkably common in the elderly. Its major clinical consequences include intracerebral hemorrhages (ICH) typically in lobar location, functional dependence (disability) and cognitive impairment.

Cortical superficial siderosis (cSS) is a common finding in CAA patients and can even be the only magnetic resonance imaging sign of CAA. cSS is of high prognostic relevance regarding future intracerebral haemorrhage and disability. Previous studies suggest that cSS is caused by recurrent focal subarachnoid hemorrhages (fSAH). However, the exact mechanisms and the temporal dynamics of this highly relevant imaging finding are largely unknown.

In addition to hemorrhagic manifestations, such as cSS, CAA patients also show ischemic lesions. Of particular interest are acute ischemic lesions as detected by diffusion imaging, which seem to be highly prevalent. Since haemorrhagic and ischemic lesions require fundamentally different therapeutic strategies, understanding the relevance and interplay of both lesion types is highly important for clinical decision making.

The HIFI-CAA cohort study aims to provide novel insights into cSS, acute ischemic lesions and other relevant brain alterations in CAA through high-frequency (monthly) serial magnetic resonance imaging.

Eligibility

Sex
ALL
Min age
50 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Probable CAA according to the modified Boston criteria with evidence of 1. cSS or fSAH 2. lobar ICH survivors without cSS or fSAH * Absence of ICH or microbleed in deep locations (basal ganglia, thalamus, brain stem) * Absence of infratentorial siderosis or infratentorial SAH * MR-/CT-/DS-angiography without evidence of cerebral aneurysm, AVM, AV-fistula or other possible etiology for the observed haemorrhagic manifestations * No history of head trauma resulting in loss of consciousness or radiologically visible traumatic brain injury * Written informed consent by patient herself/himself prior to study enrolment Exclusion Criteria: * Unwillingness to participate in high-frequency (monthly) follow-up * Severe medical condition with expected life expectancy \<1 year * Contraindications for MRI (following local guidelines of the respective study center)

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
DZNE/Bonn - Klinik und Poliklinik für Neurologie, Universitätsklinikum Bonn Bonn Germany
DZNE/Magdeburg - Universitätsklinikum Magdeburg Magdeburg Germany
Insitute for Stroke and Dementia Research Munich Germany

More Martin Dichgans trials in Germany

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06128824 on ClinicalTrials.gov ↗ ← All trials in Germany