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Clinical Trial Summary

Due to the high thrombotic risk during the atrial fibrillation procedure, new guidelines have been proposed to maintain direct oral anticoagulant therapy during the perioperative period. This resulted in a significant change in the activated clotting time (ACT) at the beginning of the procedure, making it difficult to assess the level of heparinization during the procedure. The main objective of this study was to evaluate the correlation between laboratory hemostatic parameters, ACT and the dose of unfractionated heparin received. The secondary objective of this study was to correlate these results with hemorrhagic or thrombotic complications.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05128110
Study type Observational
Source University Hospital, Strasbourg, France
Contact Charles-Ambroise TACQUARD, MD
Phone 33 3 69 55 16 08
Email [email protected]
Status Recruiting
Start date January 1, 2021
Completion date December 31, 2021

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