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NCT04679987 Clinical Trial

Incidence of Paroxysmal Atrial Fibrillation (AF) in Patients With Acute Ischemic Stroke or Transient Ischemic Attacks (TIAs) by 48 Hours Holter Monitoring

Transient Ischemic Attack Clinical Trial

Official title:
Incidence of Paroxysmal Atrial Fibrillation (AF) in Patients With Acute Ischemic Stroke or Transient Ischemic Attacks (TIAs) by 48 Hours Holter Monitoring

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04679987
Other study ID # AFTIA
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 1, 2019
Est. completion date December 1, 2020

Study information
Verified date December 2020
Source Helwan University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

200 patients presenting with symptoms of acute ischemic stroke or transient ischemic attack were included. All patients free of AF on presentation underwent 48 hours Holter monitoring within one week.

Recruitment information / eligibility
Status Completed
Enrollment 200
Est. completion date December 1, 2020
Est. primary completion date October 1, 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria: - patient with acute ischemic stroke or TIAs (within one week of onset) Exclusion Criteria: - history of persistent AF - initial ECG is AF - primary hemorrhagic stroke - acute large vessel dissection - inability or refusal of consent

Study Design

Related Conditions & MeSH terms

Intervention

Diagnostic Test:
• Holter ECG
all patients will be monitored for paroxysmal Af by holder ECG

Locations
Country Name City State
Egypt Mohamed Badr Cairo

Sponsors (1)
Lead Sponsor Collaborator
Helwan University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary presence of paroxysmal Af incidence of paroxysmal Af after TIA March 2019 -November 2020
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