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Article History

Received: 22 February 2017

Accepted: 19 October 2018

First Online: 8 November 2018

Authors’ information

: CGR is a physical therapist and PhD student at the University of Copenhagen, Faculty of Health and Medical Sciences, and is employed at the department of neurorehabilitation/TBI unit in the Research Unit on BRain Injury Copenhagen (RUBRIC). JM is a medical doctor at the Syncope Centre, Bispebjerg & Frederiksberg Hospital, Nordre Fasanvej 57, 2000 Frederiksberg, Denmark. JL is a clinical research consultant, MSc, at the Copenhagen Trial Unit, Centre for Clinical Intervention Research, Dept. 7812, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, DK-2100 Copenhagen, Denmark. CG is a medical doctor, consultant, and head of department, DMSc, at the Copenhagen Trial Unit, Centre for Clinical Intervention Research, Blegdamsvej 9, DK-2100 Copenhagen, Denmark. KM is a medical doctor, consultant, and professor at the Department of Neuroanaesthesiology, Rigshospitalet, Blegdamsvej 9, 2100 København Ø, Denmark.

: This trial has been approved by the Scientific-Ethics Committee of the Capital Region (H-16041794) and is registered at (ClinicalTrials.gov identifier: NCT02924649). After a patient is found to be eligible for the trial, informed consent from the proxy and a trial guardian (a physician not involved in the trial) is obtained by CGR. CGR is the project manager and is responsible for collecting and storing data and all correspondence.The trial is carried out in accordance with the principles of the Helsinki Declaration. The project manager is responsible for informing the Scientific-Ethics Committee of the Capital Region in Denmark of any critical adverse event or major changes of the protocol or both. All correspondence will be filed by the project manager.

: Not applicable.

: The authors declare that they have no competing interests.

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