RECRUITING

A Feasibility Study for Randomization of Code Stroke Imaging Strategies

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

• Code Stroke Imaging (CSI): MRI Or CT As First Scan For Acute Stroke Evaluation And Management

Quick Facts

Study Start:2023-10-23
Study Completion:2025-07-10
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06270927

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 120 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Age ≥ 18 years
  2. * Time last known well to presentation ≤ 24 hours
  3. * Code-stroke (suspected treatable ischemic stroke) called prior to or upon arrival to Emergency Department
  4. * Presenting to Emergency Department for first time during study period
  1. * Transfer patients
  2. * Contraindication for brain perfusion scan
  3. * Prior inclusion in study

Contacts and Locations

Study Contact

Adrienne N Dula, PHD
CONTACT
5124955922
adrienne.dula@austin.utexas.edu

Study Locations (Sites)

Ascension Seton
Austin, Texas, 78712
United States

Collaborators and Investigators

Sponsor: University of Texas at Austin

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-10-23
Study Completion Date2025-07-10

Study Record Updates

Study Start Date2023-10-23
Study Completion Date2025-07-10

Terms related to this study

Keywords Provided by Researchers

  • Stroke
  • Neuroimaging

Additional Relevant MeSH Terms

  • Brain Ischemia