Atherosclerosis Cardiovascular Disease, Carotid Arteriosclerosis, Carotid Artery Plaque, Stroke (CVA) or TIA
Conditions
Keywords
Internal Carotid Artery, Molecular Imaging, Atherosclerosis, Inflammation, PET/MRI, SST2, [18F]AlF-NOTA-octreotide, Stroke/TIA
Brief summary
This clinical trial aims to evaluate whether \[¹⁸F\]AlF-OC PET/MRI can characterize and quantify inflammation in carotid atherosclerotic plaques. The study will assess if tracer uptake in culprit and non-culprit carotid arteries, measured by standardized uptake values (SUV), is associated with future cerebrovascular events. Specifically, it will examine whether \[¹⁸F\]AlF-OC uptake predicts the risk of recurrent ipsilateral TIA, amaurosis fugax, stroke, or other vascular complications. Participants will undergo \[¹⁸F\]AlF-OC PET/MRI and will be followed via telephone interviews at 90 days, 1 year, and 3 years after their initial stroke or TIA.
Detailed description
Our study aims to assess the potential of molecular imaging with \[18F\]AlF-OC PET/MRI to characterize and quantify carotid atherosclerotic disease manifestations in patients with a recent stroke/TIA in the carotid artery territory. Eligible patients should have ≥30% stenosis in the ipsilateral carotid artery, as diagnosed by routine CTA. Additionally, we will evaluate the role of \[18F\]AlF-OC PET/MRI in risk stratification for recurrent events of patients with carotid artery stenosis and recent TIA/stroke. This study is a single center study conducted at University Hospitals Leuven in Belgium. In a first part of this study, five patients will undergo serial \[18F\]AlF-OC PET/MRI at 60, 120 and 180 minutes after injection of 4 MBq/kg \[18F\]AlF-OC for protocol optimization and methodology refinement. In the second part of this trial, patients will undergo \[18F\]AlF-OC PET/MRI at the timepoint deemed as optimal based on the findings from the first part. All subjects will be required to undergo a screening and baseline assessment, an imaging visit (\[18F\]AlF-OC PET/MRI) and three follow-up visits (telephone interview at 90 days, 1 year and 3 years after the initial stroke onset). The primary outcome is the quantification of \[18F\]AlF-OC uptake in the carotid artery by measures of standardized uptake value (SUV). For every patient, both culprit (recent symptomatic event in ipsilateral carotid artery territory) and non-culprit (recent symptomatic event in the contralateral carotid artery territory) carotid arteries will be assessed. Secondary outcomes include the predictive value of baseline plaque SUV and TBR for the recurrence of ipsilateral TIA, amaurosis fugax and stroke during 3 years follow-up, the recurrence of all stroke/TIA, the occurrence of any vascular complication (stroke/TIA, myocardial infarction, cardiac arrest, hospitalisation for unstable angina or vascular death) and the occurrence of all-cause mortality.
Interventions
DRUG[18F]AlF-OC
Participants received a single intravenous (IV) bolus injection of 4 MBq/kg \[¹⁸F\]AlF-OC (Al¹⁸F-1,4,7-triazacyclononane-1,4,7-triacetate-octreotide), followed by a flush with 0.9% NaCl.
Sponsors
Universitaire Ziekenhuizen KU Leuven
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Participant is aged over 18 years. 2. Voluntary written informed consent of the participant or their legally authorized representative has been obtained prior to any screening procedure 3. CT angiography imaging at baseline should be available as part of routine care 4. Participant is diagnosed with a recent ischemic stroke or high-risk TIA (ABCD2 ≥ 4) in the carotid artery territory and ≥ 30% carotid artery stenosis. The stroke/TIA has occurred no more than 21 days prior to tracer administration.
Exclusion criteria
1. Female who is pregnant or breast-feeding 2. Participants with a cardio-embolic stroke, small vessel stroke or other defined stroke etiology according to the TOAST classification (23) 3. Participant has a previous or ongoing recurrent or chronic disease at high risk to interfere with the performance or evaluation of the trial, according to the judgment of the investigator 4. Participants treated with carotid endarterectomy or carotid artery stenting within the past year 5. Subject has a contra-indication for or cannot tolerate MR scanning 6. Subject has an impaired renal function estimated glomerular filtration rate (eGFR) \< 40 ml/min/1.73m² (the last known value may not date from more than 3 months prior to the study PET/MR; if not available a blood analysis may be performed as part of the trial) 7. Concurrent treatment with corticosteroids and/or somatostatin analogues 8. Subject is unwilling or unable to perform all of the study procedures, or is considered unsuitable in any way by the principal investigator
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Quantification of ICA [18F]AlF-OC uptake | 1 hour post-injection | Quantification of \[18F\]AlF-OC uptake in the culprit and non-culprit carotid artery by measures of standardized uptake value (SUV) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Recurrence of ipsilaterial TIA, stroke or amaurosis fugax | 90 days, 1 year and 3 years after index event | Recurrence of ipsilateral TIA, amaurosis fugax and stroke during follow-up |
| Recurrence of all stroke/TIA | 90 days, 1 year and 3 years after the index event | Recurrence of all stroke/TIA during follow-up |
| Occurence of major adverse cardiovascular events (MACE) | 90 days, 1 year and 3 years after index event | Occurence of any vascular complication (stroke/TIA, myocardial infarction, cardiac arrest, hospitalisation for unstable angina or vascular death) during follow-up |
| Occurence of all-cause mortality | 90 days, 1 year, 3 years after index event | Occurence of all-cause mortality during follow-up |
Countries
Belgium
Contacts
Primary ContactRobin Lemmens, MD PhD
Backup ContactLouise Maes, MD
Outcome results
None listed