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RedStroke- Reducing Europe's stroke incidence: Highly cost-effective population screening programs for Atrial Fibrillation coupled with high diagnostic yield confirmation services.;Multicentre, international, investigator-initiated, controlled, randomised, double-blind clinical validation study of a smartphone application as screening tool for differentiation between sinus rhythm and atrial fibrillatio

Recruiting
Conditions
Artrial fibrillation
10007521
Registration Number
NL-OMON52879
Lead Sponsor
niversity Hospital Basel ( Switserland)
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

signed informed consent
• CHA2DS2-VASc score * 3, if patients less than 65 years old
• CHA2DS2-VASc score * 2, if patients 65 years or more

Exclusion Criteria

• history of AF
• current anticoagulation treatment,
• cardiac implanted electronic device (ICD or/and PM)

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary endpoint of this study is the prevalence of AF confirmed by ECG in<br /><br>the app group compared with the standard care group</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>The main secondary study outcomes are costs related to the AF screening with<br /><br>the app and the compliance in each study group </p><br>
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