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Stroke Patient Triage and Healthcare Provider Notification Effectiveness of Reducing Time to Initiation of Emergency Cerebral Vascular Occlusion Treatment Using AI Solution Heuron StroCare Suite™: A Prospective, Retrospective, Controlled, Multicenter Study

Stroke Patient Triage and Healthcare Provider Notification Effectiveness of Reducing Time to Initiation of Emergency Cerebral Vascular Occlusion Treatment Using AI Solution Heuron StroCare Suite™: A Prospective, Retrospective, Controlled, Multicenter Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0011971
Enrollment
480
Registered
2026-05-13
Start date
2025-10-22
Completion date
Unknown
Last updated
2026-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Chonnam National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Participants meeting all of the following criteria will be included: 1. Adults aged =19 years 2. Patients who presented to the emergency department within 24 hours of symptom onset 3. Patients who underwent non-contrast CT for suspected stroke 4. Patients diagnosed with acute ischemic stroke 5. Patients who received intravenous thrombolysis (tPA) or mechanical thrombectomy (MT) 6. (Post-AI cohort) Patients managed with the application of the Heuron StroCare Suite™ AI solution 7. (Pre-AI cohort) Patients from the period prior to the application of the AI solution

Exclusion criteria

Exclusion criteria: Participants meeting any of the following criteria will be excluded: 1. Patients younger than 19 years 2. Unknown time of symptom onset or presentation beyond 24 hours 3. Patients with symptoms caused by conditions other than stroke 4. Patients diagnosed with hemorrhagic stroke (e.g., intracerebral hemorrhage, subarachnoid hemorrhage) 5. Patients who did not undergo non-contrast CT or have insufficient imaging data 6. Missing key clinical or time-related data (e.g., arrival time, imaging time, treatment time) 7. Patients who did not receive intravenous thrombolysis (tPA) or mechanical thrombectomy (MT) 8. Any other cases deemed inappropriate by the investigator

Design outcomes

Primary

MeasureTime frame
Change in door-to-treatment time from emergency department arrival to initiation of intravenous thrombolysis (tPA) or mechanical thrombectomy (MT)

Secondary

MeasureTime frame
Sensitivity and specificity of the AI solution for detecting large vessel occlusion;Time from imaging acquisition to interpretation;Change in NIHSS(National Institutes of Health Stroke Scale) score;Modified Rankin Scale (mRS) at discharge

Countries

Korea, Republic of

Contacts

Public ContactAHN NA KOO

Chonnam National University Hospital

hello.anna9@gmail.com+82-62-220-4997

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: May 22, 2026