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SEarchiNg BiomarkErs Cerebral Amyloid Angiopathy (SENECA)

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Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta

Status

Enrolling

Conditions

Cerebral Amyloid Angiopathy

Treatments

Other: CAA patients data collection

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Cerebral amyloid angiopathy (CAA) is one of the major types of cerebral small vessel disease, and a leading cause of spontaneous intracerebral hemorrhage and cognitive decline in elderly patients. Although increasingly detected, a number of aspects including the pathophysiology, the clinical and neuroradiological phenotype and the disease course are still under investigation. The incomplete knowledge of the disease limits the implementation of evidence based guidelines on patient's clinical management and the development of treatments able to prevent or reduce disease progression.

The SENECA (SEarchiNg biomarkErs of Cerebral Angiopathy) project is the first Italian multicentre cohort study aimed at better defining the disease natural history and identifying clinical and neuroradiological markers of disease progression. By a multidisciplinary approach and the collection of a large and well phenotyped series and biorepository of CAA patients, the study is ultimately expected to improve the diagnosis and the knowledge of CAA pathophysiological mechanisms.

Full description

The SENECA is an Italian multicenter network integrating the experience of neurologists, neuroradiologists, neuro-ophthalmologists and biologists and allowing the standardized collection of a well-characterized wide series of sporadic and familial CAA patients.

Enrollment

500 estimated patients

Sex

All

Ages

55+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All consecutive patients ≥55 years (with the exception of genetic cases), referred to the participating centres, with a diagnosis of possible probable and definite symptomatic or asymptomatic CAA, defined according to the modified Boston neuroradiological criteria, who had undergone at least one brain MRI (mandatory requirement for inclusion of the patient in the study) will be recruited.

Exclusion criteria

  • evidence of other causes of cerebral hemorrhage (brain tumors, arteriovenous malformations, aneurysms, cavernous angiomas), contraindications to brain MRI, pregnancy and breastfeeding

Trial design

500 participants in 1 patient group

Cerebral amyloid angiopathy (CAA)
Description:
Cerebral amyloid angiopathy (CAA) patients
Treatment:
Other: CAA patients data collection

Trial contacts and locations

1

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Central trial contact

Renato Mantegazza, MD; Anna Bersano, MD, Phd

Data sourced from clinicaltrials.gov

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