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A Feasibility Study for Randomization of Code Stroke Imaging Strategies

NCT06270927 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2026-05-01

No results posted yet for this study

Summary

The purpose of this study is to test feasibility of a comparative effectiveness framework for acute stroke imaging using prospective electronic health data. This is a prospective, cohort feasibility study of patients presenting to the Emergency Department with suspected acute ischemic stroke. The clinical stroke team will not be blinded to the imaging modality given the nature and purpose of the interventions/imaging. Knowledge of the imaging modality used and the knowledge gained from the resulting data will need to be considered for treatment decisions. Blinding will be maintained for data abstraction and analyses. Analysis will be on an "intent-to-scan" basis and all qualifying patients will be included in their assigned cohort.

Conditions

  • Brain Ischemia

Interventions

DIAGNOSTIC_TEST

MRI

neuroimaging using MRI scanner

DIAGNOSTIC_TEST

CT

neuroimaging using CT scanner

Sponsors & Collaborators

  • Lone Star Stroke Research Consortium

    collaborator UNKNOWN

  • Ascension Texas

    collaborator UNKNOWN

  • University of Texas at Austin

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
120 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-10-23
Primary Completion
2025-12-30
Completion
2026-05-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06270927 on ClinicalTrials.gov