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. 2018 Feb 20;19:127. doi: 10.1186/s13063-018-2480-3

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© The Author(s). 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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Fig. 1 — PACER trial (Consolidated Standards of Reporting Trials (CONSORT)) Diagram. CONSORT diagram of PACER. For haematologic patients, informed consent is required prior to randomisation. For the intensive care patients, randomisation takes place via deferred consent. If consent is not obtained, data are excluded