Feasibility of comparing imaging strategies for acute stroke
• Code Stroke Imaging (CSI): MRI Or CT As First Scan For Acute Stroke Evaluation And Management
University of Texas at Austin · NCT06270927
This study is testing different imaging methods for people who might have an acute stroke to see which one works best for their treatment.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 600 (estimated) |
| Ages | 18 Years to 120 Years |
| Sex | All |
| Sponsor | University of Texas at Austin (other) |
| Locations | 1 site (Austin, Texas) |
| Trial ID | NCT06270927 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the feasibility of a comparative effectiveness framework for imaging strategies in patients with suspected acute ischemic stroke. It involves a prospective cohort of patients presenting to the Emergency Department, where the clinical stroke team will utilize standard imaging modalities while maintaining blinding for data analysis. All patients will receive standard-of-care therapy based on established clinical guidelines, and the analysis will be conducted on an 'intent-to-scan' basis, including all qualifying patients in their assigned imaging cohort.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who present with symptoms suggestive of stroke within 24 hours of their last known well time.
Not a fit: Patients who are transferred from other facilities or have contraindications for brain perfusion scans may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance the effectiveness of imaging strategies in acute stroke management, potentially leading to better patient outcomes.
How similar studies have performed: While this approach is novel in its specific framework, similar studies have shown promise in improving stroke imaging strategies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age ≥ 18 years * Time last known well to presentation ≤ 24 hours * Code-stroke (suspected treatable ischemic stroke) called prior to or upon arrival to Emergency Department * Presenting to Emergency Department for first time during study period Exclusion Criteria: * Transfer patients * Contraindication for brain perfusion scan * Prior inclusion in study
Where this trial is running
Austin, Texas
- Ascension Seton — Austin, Texas, United States (RECRUITING)
Study contacts
- Study coordinator: Adrienne N Dula, PHD
- Email: adrienne.dula@austin.utexas.edu
- Phone: 5124955922
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Brain Ischemia, Stroke, Neuroimaging