ClinicalTrials.gg
Not yet recruitingNCT07896889SCOPE-CTUpdated Oct 27, 2026

Cardiac CT Angiography in Acute Stroke Imaging (SCOPE-CT)

An interventional study of Cardiac CT Angiography in Acute Ischemic Stroke and Transient Ischemic Attacks, sponsored by Ottawa Hospital Research Institute. Not yet recruiting at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-27.

Sponsored by Ottawa Hospital Research Institute · Not applicable, Interventional, and Diagnostic

Updated Oct 27, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

Stroke can occur when a blood clot travels to the brain and blocks blood flow. In some patients, these blood clots may originate in the heart. Standard emergency stroke imaging typically includes a CT scan of the head and CT angiography (CTA) of the head and neck, but does not routinely include imaging of the heart.

This study will evaluate whether cardiac CT angiography (CTA) can be safely added to the standard acute stroke imaging workflow without delaying urgent stroke care. Participants with suspected acute ischemic stroke or high-risk transient ischemic attack (TIA) will undergo either prospective ECG-gated cardiac CTA or non-ECG-gated cardiac CTA during their acute stroke imaging examination.

The primary goal of the study is to assess the feasibility of integrating cardiac CTA into routine stroke imaging by evaluating workflow impact, image quality, radiation exposure, contrast use, and protocol completion. Findings from this study may help improve the identification of cardiac sources of stroke and inform the design of future larger studies.

Read the detailed description

Acute ischemic stroke may result from thromboembolic material originating from the heart or thoracic aorta. Current emergency stroke imaging protocols routinely include non-contrast head CT and CT angiography (CTA) of the head and neck but do not routinely include dedicated cardiac imaging during the hyperacute phase of stroke assessment.

Cardiac CT angiography (CTA) has emerged as a promising non-invasive method for identifying potential cardioembolic sources, including left atrial appendage thrombus, left ventricular thrombus, and aortic atherosclerotic disease. Earlier identification of these findings may improve diagnostic evaluation and facilitate future treatment planning.

SCOPE-CT is a prospective, single-centre feasibility pilot study evaluating the integration of cardiac CTA into the acute stroke imaging workflow at The Ottawa Hospital. Approximately 50 participants with suspected acute ischemic stroke or high-risk transient ischemic attack (TIA) will undergo either prospective ECG-triggered cardiac CTA or non-ECG-gated cardiac CTA in addition to standard stroke imaging.

The primary objective is to determine whether cardiac CTA can be incorporated into the hyperacute stroke imaging pathway without clinically meaningful disruption of workflow. Secondary objectives include assessment of image quality, protocol completion rates, radiation dose, contrast utilization, workflow impact, and detection of potential cardioembolic sources.

The results of this pilot study will be used to inform protocol optimization and the design of future larger studies evaluating the role of cardiac CTA in acute stroke assessment.

02

Conditions studied

  • Acute Ischemic Stroke and Transient Ischemic Attacks

Keywords

  • Cardiac CT Angiography
  • ECG-Gated Cardiac CTA
  • Acute Ischemic Stroke
  • Transient Ischemic Attack
  • SCOPE-CT
03

In context

Ischemic Stroke

2,612 studies on the registry are indexed under Ischemic Stroke; 971 are open to participants now.

This study's planned enrollment of 50 is below the median of 120 across 1,776 interventional studies indexed under Ischemic Stroke.

Browse Ischemic Stroke studies →

Lead sponsor

Ottawa Hospital Research Institute is the lead sponsor of 547 studies on the registry; 99 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult patients presenting with suspected acute ischemic stroke or who undergo standard acute stroke CT/CTA imaging.
  • Age ≥18 years.
  • Suspected acute ischemic stroke or high-risk TIA.
  • Undergoing standard-of-care acute stroke CT/CTA.
  • Presentation within a acute stroke imaging window, ≤24 hours from last-known-well.
  • Able to undergo iodinated contrast-enhanced CTA

Exclusion criteria

Exclusion Criteria:

  • Known to iodinated contrast.
  • Severe renal impairment where additional contrast is deemed clinically inappropriate.
  • Hemodynamic instability precluding additional imaging.
  • Pregnancy.
  • Severe motion/agitation where imaging is not feasible.
  • Prior enrollment in the study.
  • The treating stroke/radiology team determines that additional cardiac CTA is not appropriate.
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

TIA (transient ischaemic attack)

A “mini-stroke”: temporary stroke-like symptoms caused by reduced blood flow to part of the brain, spinal cord or eye, without signs of a new stroke on a scan.

Stroke symptoms need emergency care at once, even if they go away.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
50 participants (estimated)

Study arms

  • Experimental
    ECG-Gated Cardiac CT Angiography

    Participants undergo prospective ECG-gated cardiac CT angiography (CTA) during acute stroke imaging to evaluate potential cardiac and aortic sources of embolism and assess feasibility within the acute stroke workflow.

    Diagnostic Test: Cardiac CT Angiography

  • Experimental
    Non-ECG-Gated Cardiac CT Angiography

    Participants undergo non-ECG-gated cardiac CT angiography (CTA) during acute stroke imaging. This imaging approach extends the standard stroke CTA acquisition to include the heart and thoracic aorta without ECG synchronization. The study will evaluate the feasibility, image quality, workflow impact, radiation exposure, and diagnostic performance of this approach within the acute stroke workflow.

    Diagnostic Test: Cardiac CT Angiography

Interventions

  • Diagnostic testCardiac CT Angiography

    Cardiac CT angiography performed during acute stroke imaging using prospective ECG triggering to synchronize image acquisition with the cardiac cycle. This approach is intended to improve visualization of cardiac structures, including the left atrial appendage and left ventricle, while minimizing radiation exposure. The study will evaluate the feasibility of integrating this imaging protocol into the acute stroke workflow. Cardiac CT angiography performed during acute stroke imaging without ECG synchronization. This approach extends the standard stroke CT angiography acquisition to include the heart and thoracic aorta with minimal additional imaging time. The study will evaluate the feasibility, image quality, workflow impact, and diagnostic performance of this imaging protocol within the acute stroke workflow.

06

What researchers measure

Primary outcomes

  1. Feasibility of Integrating Cardiac CT Angiography Into the Acute Stroke Imaging Workflow

    Feasibility will be assessed by successful completion of the cardiac CT angiography protocol and its integration into the acute stroke imaging workflow without clinically meaningful disruption to patient care.

    Time frame: During the acute stroke imaging encounter (Day 1)

  2. Additional Scanner/Table Time

    Additional scanner/table time associated with the cardiac CT angiography acquisition compared with the standard acute stroke imaging workflow.

    Time frame: Day 1

Secondary outcomes

  1. Assessment of diagnostic image quality for cardiac CT angiography acquisitions.

    Diagnostic image quality of cardiac CT angiography (CTA) acquisitions will be assessed by study investigators and radiologists to determine whether the images are of sufficient quality for evaluation of potential cardiac and aortic sources of embolism. Image quality assessments will include the presence of motion artifact, visualization of relevant cardiac structures, and overall diagnostic interpretability.

    Time frame: During the imaging procedure (Day 1)

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No — Individual participant data will not be shared outside the study team. Data will be stored and managed in accordance with institutional privacy and confidentiality requirements.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 27, 2026
Show all 1 update
  1. Oct 27, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07896889
Responsible party
Sponsor
First posted
Oct 27, 2026
Start date
Oct 26, 2026 (estimated)
Primary completion
Oct 31, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Oct 27, 2026

Study contacts

Eduardo Portela de Oliveira, MD
Contact
eporteladeoliveira@toh.ca
613-798-5555
Rafael Ochoa Sanchez, PhD
Contact
raochoa@ohri.ca
613-798-5555 ext. 10912
Alice Black, Manager
study director · Ottawa Hospita Research Institute

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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