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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04330222
Other study ID # A095132
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 9, 2020
Est. completion date January 12, 2024

Study information

Verified date September 2022
Source University of Cambridge
Contact Stefania Nannoni, MD
Phone 01223 216 509
Email sn572@medschl.cam.ac.uk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

CamSVD is jointly sponsored by the University of Cambridge and Cambridge University Hospitals NHS Foundation Trust. We aim to explore and understand the underlying arterial pathology in Cerebral Small Vessel Disease (SVD) using ultra-high-field 7 Tesla MRI. We will optimise 7T Time-of-Flight MR angiography, blood suppressed MR sequence and phase-contrast (PC) MR angiography for visualization of perforating lenticulostriate arteries. This optimised sequences will be used to determine the range of arterial pathologies seen in individuals presenting with lacunar strokes. The pathologies of the perforating lenticulostriate arteries will be correlated with conventional clinical risk factors, cognition and radiological markers of SVD.


Recruitment information / eligibility

Status Recruiting
Enrollment 210
Est. completion date January 12, 2024
Est. primary completion date January 12, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: 1. Symptomatic lacunar stroke with corresponding lacunar infarct on MRI Exclusion Criteria: 1. Unable/unwilling to consent; 2. Age<18; 3. Stroke aetiology due to cardio-embolism or large vessel disease; 4. Lacunar infarcts >1.5cm; 5. Severe stroke (NIHSS score =16); 6. Evidence of cortical infarct of any size; 7. Other major neurological diseases; 8. Severe systemic diseases such as heart failure, liver failure and kidney failure or any illness in the judgement of the investigator that could affect participation in the study; 9. MRI contraindications e.g. metal objects in or on the body, claustrophobia, pregnancy, known allergy to gadolinium containing contrast agent, impaired renal function with estimated glomerular filtration rate (eGFR) <59ml/min/1.73m2.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
7 Tesla Magnetic Resonance Imaging
Diagnostic Imaging
Other:
Brief Memory and Executive Test
Cognitive Assessment

Locations

Country Name City State
United Kingdom University of Cambridge Cambridge Cambridgeshire

Sponsors (3)

Lead Sponsor Collaborator
University of Cambridge Cambridge University Hospitals NHS Foundation Trust, Wolfson Brain Imaging Centre

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Range and pattern of pathology seen in the perforating arteries like presence or absence of focal atheroma and narrowing March 2020-
Secondary Differences in morphology of perforating arteries between SVD patients and healthy volunteers March 2020-
Secondary Correlation of morphology of perforating arteries with cardiovascular risk factors and radiological markers of SVD March 2020-
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