Geest, Vincent http://orcid.org/0000-0001-5777-331X
Steffen, Paul
Winkelmeier, Laurens
Faizy, Tobias D.
Heitkamp, Christian
Kniep, Helge
Meyer, Lukas
Zelenak, Kamil
Götz, Thomalla
Fiehler, Jens
Broocks, Gabriel
Funding for this research was provided by:
Universitätsklinikum Hamburg-Eppendorf (UKE)
Article History
Received: 31 October 2023
Revised: 31 January 2024
Accepted: 17 February 2024
First Online: 16 April 2024
Declarations
:
: The scientific guarantor of this publication is Gabriel Broocks.
: The authors of this manuscript declare no relationships with any companies, whose products or services may be related to the subject matter of the article.
: Götz Thomalla reports funding from the European Commission; personal consulting fees from Acandis, AstraZeneca, Bayer, Boehringer lngelheim, and Stryker; personal payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing, or educational events from Acandis, Alexion, Marin, Bayer, Boehringer lngelheim, BristolMyersSquibb/Pfizer, Daiichi Sankyo, and Stryker; participation as DSMB member for the TEA Stroke Trial (no payments) and ReSClnD trial (no payments); work as a speaker of the Commission for Cerebrovascular Diseases of the German Society of Neurology (DGN; no payments); and membership of the Board of Directors of the European Stroke Organisation (ESO; no payments). Jens Fiehler reports funding from the European Commission; personal consulting fees from Acandis, Cerenovus, Medtronic, Microvention, Phenox, Stryker, and Roche; consulting at Philips (no payments); payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from Penumbra and Tonbridge; support for attending meetings or travel from Medtronic and Penumbra; stock or stock options from Tegus Medical, Eppdata, and Vastrax; and participation in a Data Safety Monitoring Board or Advisory Board at Phenox (personal fees) and Stryker (personal fees) and is a past president of ESMINT.
: Statistical analyses of this manuscript were performed by the authors without external advice.
: Written informed consent was not required for this study because of the study design.
: Institutional Review Board approval was obtained.
: No overlap.
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