Clinico-radiological Correlations in Cerebro-VASCULAR Disease

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorIRCCS San Raffaele

About this trial

This observational retrospective and prospective registry aims to explore the relationships between clinical manifestations and radiological findings in cerebrovascular diseases. These conditions are characterized by heterogeneous radiological presentations and different etiologies, posing challenges for accurate diagnosis and effective treatment. Understanding these correlations is essential for advancing diagnostic accuracy and therapeutic strategies.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age Range: 18-100 years old.

Must have undergone a CT or MRI scan of the central nervous system (CNS) (for clinical reasons).

Disqualifiers

Alternative diagnosis to vascular pathology that explains clinical symptoms.

MRI or CT non-diagnostic or non-evaluable MRI due to motion artifacts.

Trial population

The registry will focus on adults aged 18 to 100 of both genders diagnosed with various cerebrovascular diseases based on clinical and imaging evaluations. Participants will be selected from a retrospective registry of patients who have undergone MRI or CT scans for clinical indications. In addition to the retrospective cohort, the registry will also include a prospective component, enrolling newly diagnosed patients who meet the same eligibility criteria.

Trial design

Design model

Other

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Proportion of patients with each key MRI/CT finding in cerebrovascular disease (lesion location, vessel involvement, hemorrhagic transformation)

Primary Outcome Measure: Diagnostic imaging trends in cerebrovascular disease Description: Key imaging findings from first MRI/CT (e.g., lesion location, vessel involvement; %).

Time frame
Baseline (at diagnosis), up to 20 years

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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