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OpenTrials
Completed

NCT Number: NCT04679987

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

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Holter ECG

Diagnostic Test

all patients will be monitored for paroxysmal Af by holder ECG

Primary outcomes

  1. presence of paroxysmal Af

    Time frame: March 2019 -November 2020

    incidence of paroxysmal Af after TIA

Sponsors and collaborators

Lead sponsor

Helwan University

Other

Registry information

Important dates

Study start
2019
Primary completion
2019
Study completion
2020
First posted
Dec 22, 2020
Registry last updated
Dec 28, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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