- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07493694
Clinico-radiological Correlations in Cerebro-VASCULAR Disease
March 25, 2026 updated by: Anna del Poggio, IRCCS San Raffaele
Clinico-radiological Correlations in Cerebro-VASCULAR Disease: Toward a BetteR understAndINg of Their Heterogeneous Manifestations in a Retrospective and Prospective Observational Registry
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.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
1143
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study 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.
Description
Inclusion Criteria:
- Age Range: 18-100 years old.
- Must have undergone a CT or MRI scan of the central nervous system (CNS) (for clinical reasons).
Exclusion Criteria:
- Alternative diagnosis to vascular pathology that explains clinical symptoms.
- MRI or CT non-diagnostic or non-evaluable MRI due to motion artifacts.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proportion of patients with each key MRI/CT finding in cerebrovascular disease (lesion location, vessel involvement, hemorrhagic transformation)
Time Frame: Baseline (at diagnosis), up to 20 years
|
Primary Outcome Measure: Diagnostic imaging trends in cerebrovascular disease Description: Key imaging findings from first MRI/CT (e.g., lesion location, vessel involvement; %). |
Baseline (at diagnosis), up to 20 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
April 1, 2026
Primary Completion (Estimated)
April 1, 2046
Study Completion (Estimated)
April 1, 2046
Study Registration Dates
First Submitted
March 5, 2026
First Submitted That Met QC Criteria
March 20, 2026
First Posted (Actual)
March 25, 2026
Study Record Updates
Last Update Posted (Actual)
March 30, 2026
Last Update Submitted That Met QC Criteria
March 25, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Other Study ID Numbers
- VASCULAR-BRAIN
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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