Clinical Trial

Prolonged Cardiac ECG Patch Versus Conventional Holter For Detecting Atrial Fibrillation After Cerebral Ischemic Event

Study acronym: PROVE-AF
Active, Not Recruiting
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Summary
The aim of this study is to compare the diagnostic yield of water-resistant, wireless 7-day cardiac ECG patch versus conventional 24-hour Holter recording in detecting paroxysmal atrial fibrillation in patients admitted with acute ischemic stroke or transient ischemic attack of undetermined etiology after completion of a standard clinical stroke workup.
Protocol Amendment History 5 amendments
This ClinicalTrials.gov record has been amended 5 times since 2021-10-05; most recent amendment 2026-04-21.
Status change: Recruiting → Active, Not Recruiting 2024-06-01
Trial Details
NCT Number NCT05082467
Lead Sponsor Sarawak General Hospital
Collaborators: Sarawak Heart Centre, Ministry of Health, Malaysia
Conditions Stroke, Atrial Fibrillation
Enrollment 320 participants
Start Date 2021-01-12
Primary Completion 2027-08-22 (estimated)
Study Completion 2027-08-22 (estimated)
Updated on ClinicalTrials.gov 2026-04-24