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OpenTrials
Completed

NCT Number: NCT02911545

Non-vitamin K Oral Anticoagulants in Cardioversion

Non-vitamin K oral anticoagulants (NOAC) have been shown to be safe and effective alternatives to warfarin for stroke prevention in patients with nonvalvular AF (NVAF). There are yet limited real life data on outcomes following elective cardioversion in AF patients treated with NOACs. The aim of this study is to investigate the complications and the use of NOACs in AF patients undergoing cardioversion.

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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

  • AF patients undergoing cardioversion

Exclusion criteria

-

Treatment and study plan

Primary outcomes

  1. Incidence and predictors of thromboembolic complications

    Time frame: 31 days after cardioversion of persistent AF

  2. Incidence and predictors of bleeding

    Time frame: 31 days after cardioversion of persistent AF

Secondary outcomes

  1. Number of recurrence of AF

    Time frame: 31 days after cardioversion of persistent AF

  2. Hemodynamic complications of cardioversion

    Time frame: 31 days after cardioversion of persistent AF

Sponsors and collaborators

Lead sponsor

Helsinki University Central Hospital

Other

Collaborators

  • University of Turku

Registry information

Official study title

Non-vitamin K Oral Anticoagulants in Cardioversion of Atrial Fibrillation. FinCV3

Acronym: FinCV3

Important dates

Study start
2011
Primary completion
2015
Study completion
2016
First posted
Sep 22, 2016
Registry last updated
Sep 22, 2016

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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