Acute Ischemic Stroke
Conditions
Keywords
Stroke
Brief summary
The overarching objective of our proposal is to develop a One-Stop-Shop imaging using the available C-arm Cone-Beam Computed Tomography (CBCT) data acquisition systems currently widely available worldwide in interventional angiography suites to enable acute ischemic stroke patients to be imaged, triaged, treated, and assessed using a single modality in one room.
Detailed description
This is an evaluation to determine the efficacy of the use of C-arm CBCT with SMART RECON novel software for the rapid assessment of time-resolved CTA and CT perfusion in the setting of ischemic cerebrovascular events. As a leading center for the treatment of cerebrovascular disease in the Midwest as well as being one of the first Comprehensive Stroke Centers in the United States we have a large potential patient group to assess. The pilot plan is to compare conventional CT/CTA/CTP acquired during the clinical work up with C-arm CBCT/CTA/CTP acquired in the angiography suite at initiation of therapy. The C-arm CBCT acquisition provides whole brain coverage (compared to only 8 cm brain coverage with conventional CT) with less radiation and higher resolution; the CT perfusion maps obtained using C-arm CBCT and new reconstruction algorithms provides better perfusion maps.
Interventions
DIAGNOSTIC_TESTC-Arm Cone Beam Computed Tomography
C-ARM CBCT angiogram and CBCT perfusion imaging using prototype software (SMART-RECON) can rapidly and accurately assess the cerebral blood flow maps in the setting of decreased blood flow to the brain (ischemic cerebrovascular events). This rapid assessment would eliminate the need for the patient to be imaged in another scanner and be subsequently transported again to another room; all anatomic and physiologic imaging would occur in the angiography suite.
Sponsors
National Institute for Biomedical Imaging and Bioengineering (NIBIB)
University of Wisconsin, Madison
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE
Intervention model description
Single center, open label, single-arm, pilot study
Eligibility
Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No
Inclusion criteria
1. Patients with acute ischemic stroke presenting within 8 hours of onset 2. Patients that present with a large artery occlusion 3. Adults 18 years of age or older. 4. Women of childbearing potential must not be pregnant. 5. National Institutes of Health Stroke Scale (NIHSS) of \>5 6. No severe co-morbidities
Exclusion criteria
1. Women that are pregnant 2. History of severe renal disease (e.g. stage 4-5) 3. History of renal transplant
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Percent of C-arm Cone Beam CT scans that detect Hyperemia or Oligemia compared to Standard of Care conventional CT | 1 study visit up to 1 hour | To demonstrate device feasibility for phase 2 of this study, the investigators need to demonstrate that the presence of hyperemia or oligemia detected with standard of care conventional CT is also detected to a clinically acceptable degree with C-arm Cone Beam CT. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Optimization of One-Stop-Shop Imaging | Up to 24 months | Data collected will be used to optimize C-arm CBCT imaging parameters, data acquisition methods and contrast dose. |
| Analysis of Perfusion Parameters from One-Stop-Shop Perfusion Maps | Up to 24 months | Local perfusion parameters on image slices will be measured and compared against the corresponding measurements from diagnostic CTP measurements. |
| Analysis of ROIs from One-Stop-Shop Perfusion Maps | Up to 24 months | Standard deviations for a variety of regions of interest (ROIs) on image slices will be measured and compared against the corresponding measurements from diagnostic CTP measurements. |
Countries
United States
Outcome results
None listed