Protocol for a randomised controlled trial comparing warfarin with no oral anticoagulation in patients with atrial fibrillation on chronic dialysis: the Danish Warfarin-Dialysis (DANWARD) trial

Author:

Ballegaard Ellen Linnea FreeseORCID,Lindhard Kristine,Lindhardt MortenORCID,Peters Christian Daugaard,Thomsen Nielsen Finn,Tietze Ida Nørager,Borg Rikke,Boesby Lene,Bertelsen Marianne Camilla,Brøsen Julie Maria Bøggild,Cibulskyte-Ninkovic Donata,Rantanen Jesper Moesgaard,Mose Frank Holden,Kampmann Jan Dominik,Nielsen Alice Skovhede,Breinholt Johanne Kodal,Kofod Dea HaagensenORCID,Bressendorff Iain,Clausen Peter Vilhelm,Lange Theis,Køber Lars,Kamper Anne-Lise,Bang Casper Niels Furbo,Torp-Pedersen Christian,Hansen Ditte,Grove Erik L,Gislason Gunnar,Dam Jensen Jens,Olesen Jonas Bjerring,Hornum Mads,Rix Marianne,Schou Morten,Carlson Nicholas

Abstract

IntroductionAtrial fibrillation is highly prevalent in patients on chronic dialysis. It is unclear whether anticoagulant therapy for stroke prevention is beneficial in these patients. Vitamin K-antagonists (VKA) remain the predominant anticoagulant choice. Importantly, anticoagulation remains inconsistently used and a possible benefit remains untested in randomised clinical trials comparing oral anticoagulation with no treatment in patients on chronic dialysis. The Danish Warfarin-Dialysis (DANWARD) trial aims to investigate the safety and efficacy of VKAs in patients with atrial fibrillation on chronic dialysis. The hypothesis is that VKA treatment compared with no treatment is associated with stroke risk reduction and overall benefit.Methods and analysisThe DANWARD trial is an investigator-initiated trial at 13 Danish dialysis centres. In an open-label randomised clinical trial study design, a total of 718 patients with atrial fibrillation on chronic dialysis will be randomised in a 1:1 ratio to receive either standard dose VKA targeting an international normalised ratio of 2.0–3.0 or no oral anticoagulation. Principal analyses will compare the risk of a primary efficacy endpoint, stroke or transient ischaemic attack and a primary safety endpoint, major bleeding, in patients allocated to VKA treatment and no treatment, respectively. The first patient was randomised in October 2019. Patients will be followed until 1 year after the inclusion of the last patient.Ethics and disseminationThe study protocol was approved by the Regional Research Ethics Committee (journal number H-18050839) and the Danish Medicines Agency (case number 2018101877). The trial is conducted in accordance with the Helsinki declaration and standards of Good Clinical Practice. Study results will be disseminated to participating sites, at research conferences and in peer-reviewed journals.Trial registration numbersNCT03862859, EUDRA-CT 2018-000484-86 and CTIS ID 2022-502500-75-00.

Funder

Augustinus Foundation

Heart Foundation

Publisher

BMJ

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