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Not yet recruiting Not applicable Interventional

Impact of Atrial Fibrillation Prediction Model on Prescribing Oral Anti-Coagulation in Patients With Cryptogenic Stroke

ClinicalTrials.gov ID: NCT07934511

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT07934511. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 15, 2026, 8:39 AM EST

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Official title

Prediction of Atrial Fibrillation in Patients With Embolic Stroke of Unknown Source

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Stroke is a major cause of disability and the second leading cause of death in adults. Some strokes are linked to atrial fibrillation (AF), a type of irregular heartbeat. When AF is found, doctors usually prescribe blood-thinning medicines to help prevent another stroke. If AF is not found, patients are usually treated with antiplatelet medicines, such as aspirin. However, AF can be difficult to detect. Because of this, doctors may not know which treatment is best. Our research team has developed computer programs that analyze a normal electrocardiogram (EKG) and predict whether a person may develop AF in the future. These programs have been shown to be highly accurate. The goal of this study is to see how sharing these prediction results affects treatment decisions made by patients who have had an embolic stroke of undetermined source (ESUS) and their neurologist. An ESUS is a type of stroke where the exact cause cannot be identified. Participants in the study will have their normal EKG analyzed using the prediction program. Researchers will then evaluate whether providing these results to the neurologist influences decisions about the patient's care.

Study identification

NCT ID
NCT07934511
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Lead sponsor
Samir Saba
Other
Enrollment
100 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2026 (Estimated)
Primary completion
Sep 2028 (Estimated)
Completion
Oct 2028 (Estimated)
Last update posted
Nov 13, 2026

2026 – 2028

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
UPMC Pittsburgh Pennsylvania 15213 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07934511, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 13, 2026 · Synced Nov 15, 2026

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