AUTHOR=van de Munckhof Anita , Sánchez van Kammen Mayte , Krzywicka Katarzyna , Aaron Sanjith , Aguiar de Sousa Diana , Antochi Florina , Arauz Antonio , Barboza Miguel A. , Conforto Adriana B. , Dentali Francesco , Galdames Contreras Daniel , Ji Xunming , Jood Katarina , Heldner Mirjam R. , Hernández-Pérez María , Kam Wayneho , Kleinig Timothy J. , Kristoffersen Espen S. , Leker Ronen R. , Lemmens Robin , Poli Sven , Yeşilot Nilüfer , Wasay Mohammad , Wu Teddy Y. , Arnold Marcel , Lucas-Neto Lia , Middeldorp Saskia , Putaala Jukka , Tatlisumak Turgut , Ferro José M. , Coutinho Jonathan M. TITLE=Direct oral anticoagulants for the treatment of cerebral venous thrombosis – a protocol of an international phase IV study JOURNAL=Frontiers in Neurology VOLUME=14 YEAR=2023 URL=https://www.frontiersin.org/journals/neurology/articles/10.3389/fneur.2023.1251581 DOI=10.3389/fneur.2023.1251581 ISSN=1664-2295 ABSTRACT=Introduction

Current guidelines recommend that patients with cerebral venous thrombosis (CVT) should be treated with vitamin K antagonists (VKAs) for 3–12 months. Direct oral anticoagulants (DOACs), however, are increasingly used in clinical practice. An exploratory randomized controlled trial including 120 patients with CVT suggested that the efficacy and safety profile of dabigatran (a DOAC) is similar to VKAs for the treatment of CVT, but large-scale prospective studies from a real-world setting are lacking.

Methods

DOAC-CVT is an international, prospective, observational cohort study comparing DOACs to VKAs for the prevention of recurrent venous thrombotic events after acute CVT. Patients are eligible if they are 18 years or older, have a radiologically confirmed CVT, and have started oral anticoagulant treatment (DOAC or VKA) within 30 days of CVT diagnosis. Patients with an absolute contra-indication for DOACs, such as pregnancy or severe renal insufficiency, are excluded from the study. We aim to recruit at least 500 patients within a three-year recruitment period. The primary endpoint is a composite of recurrent venous thrombosis and major bleeding at 6 months of follow-up. We will calculate an adjusted odds ratio for the primary endpoint using propensity score inverse probability treatment weighting.

Discussion

DOAC-CVT will provide real-world data on the comparative efficacy and safety of DOACs versus VKAs for the treatment of CVT.

Clinical trial registration

ClinicalTrials.gov, NCT04660747.