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Cerebral Amyloid Angiopathy: Vascular Imaging and fluid markers of Amyloid deposition

Cerebral Amyloid Angiopathy: Vascular Imaging and fluid markers of Amyloid deposition - CAVIA Body fluid and imaging biomarkers for CAA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42188
Enrollment
100
Registered
2015-07-15
Start date
2016-07-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

neurodegenerative aandoeningen (vasculair) Cerebral amyloid angiopathy small vessel disease

Interventions

Biomarkers
Cerebral amyloid angiopathy
Cerebrospinal fluid
Imaging

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for sporadic CAA group: - Fulfilment of the modified Boston criteria for Cerebral Amyloid Angiopathy (CAA);Inclusion criteria for late-onset AD group: - Fulfillment of the diagnostic criteria - Available T2* MRI scan with information on presence or absence of CAA;Inclusion criteria for RUNDMC participants: - Participants in the ongoing RUNDMC study (PI dr. FE de Leeuw) will be selected for the likelihood of the presence or absence of CAA, based on T2* MRI investigations that are already available.

Exclusion criteria

Exclusion criteria: Exclusion criteria for MRI: - Metal parts in the body (pacemaker, neurostimulator, clips, medication pumps, port-a-cath, hearing aids, cochlear implants, prostheses, piercings) - Claustrofobia - Difficulty with lying down for more than 30 minutes - Pregnancy ;Exclusion criteria for Lumbar puncture: - Allergy to local anesthetic agents - Medical history of compression of spinal cord, spinal surgery, skin infection, developmental abnormalities in lower spine, blood coagulopathy, anticoagulant medication. - Clinical (or previous MRI) evidence of structural (space occupying) cerebral abnormalities that are not compatible with the performance of an LP including malignancies, abscess or obstructive hydrocephalus.

Design outcomes

Primary

MeasureTime frame
• develop and validate sensitive and specific body fluid and neuroimaging biomarkers to detect CAA during life.

Secondary

MeasureTime frame
• correlate novel neurochemical and neuroimaging biomarkers with each other and with measures of cognitive decline

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)