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. 2022 Dec 29;4(1):96–107. doi: 10.1038/s43018-022-00503-w

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© The Author(s) 2022

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — Patient flow within the RECOVER trial. ^aTwo more patients were initially randomized but were later removed from the randomization tool and database. For one patient, informed consent was lost. The other patient withdrew consent and requested the deletion of all data. ^bAll patients lost to follow-up reached the primary endpoint, as lost to follow up occurred after discharge.