Stroke Clinical Trial
Official title:
Hybrid 18F-Fluoride Positron Emission Tomography-Magnetic Resonance Imaging in Patients With Acute Acute Neurovascular Syndrome
NCT number | NCT03215563 |
Other study ID # | AC17058 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | October 12, 2017 |
Est. completion date | January 10, 2020 |
Verified date | February 2020 |
Source | University of Edinburgh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Ischaemic stroke is a major cause of death and disability worldwide. In patients with recent stroke, the 18F-fluoride positron emission tomography-computed tomography highlights high-risk culprit carotid plaque and is more discriminatory than 18F-fluorodeoxyglucose. Using hybrid positron emission tomography-magnetic resonance imaging investigators propose to build upon these findings by prospectively assessing 18F-fluoride uptake in a broad range of patients with acute transient ischaemic attack or ischaemic stroke. Investigators will specifically examine the association of 18F-fluoride uptake with multiparametric magnetic resonance imaging assessments of atherosclerotic plaque, especially the role of thrombus and lipid. Finally, using transcranial Doppler and diffusion-weighted magnetic resonance brain imaging, an assessment of the functional consequences of 18F-fluoride-positive atherosclerotic plaque will be performed. If successful, this technique has a number of valuable translational applications including the better selection of patients for carotid intervention.
Status | Completed |
Enrollment | 80 |
Est. completion date | January 10, 2020 |
Est. primary completion date | January 10, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 40 Years and older |
Eligibility |
Inclusion Criteria: 1. Patients above 40 years of age with carotid artery stenosis that do not achieve criteria for CEA (<50% for men, <70% for women, by NASCET criteria) or the patient has declined CEA. 2. Patients above 40 years of age with atherosclerotic disease of aortic arch and its branches. Exclusion Criteria: 1. Patients with new stroke and a modified Rankin score >3 2. Chronic kidney disease with an estimated Glomerular Filtration Rate (eGFR) of <30 ml/min/1.73 m2 3. Atrial fibrillation 4. Pregnant women 5. Prior ipsilateral carotid intervention 6. Prior neck radiotherapy 7. Inability to tolerate the supine position 8. Participation in the study would result in delay to surgery 9. Psychiatric illness/social situations that would limit compliance with study requirements 10. History of allergic reaction attributed to 18F-Fluoride 11. History of allergic reaction to gadolinium contrast media 12. Metal implants or devices including pacemakers and defibrillators |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Centre for Cardiovascular Science | Edinburgh |
Lead Sponsor | Collaborator |
---|---|
University of Edinburgh |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 18F-fluoride uptake in the culprit plaque in carotid, aortic and intra-cranial vessels. | 18F-fluoride uptake will be measured by the mean and max Standardised Uptake Values (SUV) derived from the culprit atherosclerotic plaques. | 2 weeks |
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