Cargando…

GLP-1 analogues for neuroprotection after out-of-hospital cardiac arrest: study protocol for a randomized controlled trial

BACKGROUND: Attenuating the neurological damage occurring after out-of-hospital cardiac arrest is an ongoing research effort. This dual-centre study investigates the neuroprotective effects of the glucagon-like-peptide-1 analogue Exenatide administered within 4 hours from the return of spontaneous c...

Descripción completa

Detalles Bibliográficos
Autores principales: Wiberg, Sebastian, Hassager, Christian, Thomsen, Jakob Hartvig, Frydland, Martin, Høfsten, Dan Eik, Engstrøm, Thomas, Køber, Lars, Schmidt, Henrik, Møller, Jacob Eifer, Kjaergaard, Jesper
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929765/
https://www.ncbi.nlm.nih.gov/pubmed/27363489
http://dx.doi.org/10.1186/s13063-016-1421-2
_version_ 1782440653090717696
author Wiberg, Sebastian
Hassager, Christian
Thomsen, Jakob Hartvig
Frydland, Martin
Høfsten, Dan Eik
Engstrøm, Thomas
Køber, Lars
Schmidt, Henrik
Møller, Jacob Eifer
Kjaergaard, Jesper
author_facet Wiberg, Sebastian
Hassager, Christian
Thomsen, Jakob Hartvig
Frydland, Martin
Høfsten, Dan Eik
Engstrøm, Thomas
Køber, Lars
Schmidt, Henrik
Møller, Jacob Eifer
Kjaergaard, Jesper
author_sort Wiberg, Sebastian
collection PubMed
description BACKGROUND: Attenuating the neurological damage occurring after out-of-hospital cardiac arrest is an ongoing research effort. This dual-centre study investigates the neuroprotective effects of the glucagon-like-peptide-1 analogue Exenatide administered within 4 hours from the return of spontaneous circulation to comatose patients resuscitated from out-of-hospital cardiac arrest. METHODS/DESIGN: This pilot study will randomize a total of 120 unconscious patients with sustained return of spontaneous circulation after out-of-hospital cardiac arrest undergoing targeted temperature management in a blinded one-to-one fashion to a 6-hour and 15-minute infusion of either Exenatide or placebo. Patients are eligible for inclusion if resuscitated from cardiac arrest with randomization from 20 minutes to 240 minutes after return of spontaneous circulation. The co-primary endpoint is feasibility, defined as the initiation of treatment within the inclusion window in more than 90 % of participants, and efficacy, defined as the area under the neuron-specific enolase curve from 0 to 72 hours after admission. Secondary endpoints include all-cause mortality at 30 days and Cerebral Performance Category as well as a modified Rankin Score at 180 days. The study has been approved by the Danish National Board of Health and the local Ethics Committee and is monitored by Good Clinical Practice units. The study is currently enrolling. DISCUSSION: This paper presents the methods and planned statistical analyses used in the GLP-1 trial and aims to minimize bias and data-driven reporting of results. TRIAL REGISTRATION: 1) Danish National Board of Health, EudraCT 2013-004311-45. Registered on 25 March 2014. 2) Videnskabsetisk komité C, Region Hovedstaden, No. 45728. Registered on 29 January 2014. 3) Clinicaltrial.gov, NCT02442791. Registered on 25 of January 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-016-1421-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-4929765
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-49297652016-07-02 GLP-1 analogues for neuroprotection after out-of-hospital cardiac arrest: study protocol for a randomized controlled trial Wiberg, Sebastian Hassager, Christian Thomsen, Jakob Hartvig Frydland, Martin Høfsten, Dan Eik Engstrøm, Thomas Køber, Lars Schmidt, Henrik Møller, Jacob Eifer Kjaergaard, Jesper Trials Study Protocol BACKGROUND: Attenuating the neurological damage occurring after out-of-hospital cardiac arrest is an ongoing research effort. This dual-centre study investigates the neuroprotective effects of the glucagon-like-peptide-1 analogue Exenatide administered within 4 hours from the return of spontaneous circulation to comatose patients resuscitated from out-of-hospital cardiac arrest. METHODS/DESIGN: This pilot study will randomize a total of 120 unconscious patients with sustained return of spontaneous circulation after out-of-hospital cardiac arrest undergoing targeted temperature management in a blinded one-to-one fashion to a 6-hour and 15-minute infusion of either Exenatide or placebo. Patients are eligible for inclusion if resuscitated from cardiac arrest with randomization from 20 minutes to 240 minutes after return of spontaneous circulation. The co-primary endpoint is feasibility, defined as the initiation of treatment within the inclusion window in more than 90 % of participants, and efficacy, defined as the area under the neuron-specific enolase curve from 0 to 72 hours after admission. Secondary endpoints include all-cause mortality at 30 days and Cerebral Performance Category as well as a modified Rankin Score at 180 days. The study has been approved by the Danish National Board of Health and the local Ethics Committee and is monitored by Good Clinical Practice units. The study is currently enrolling. DISCUSSION: This paper presents the methods and planned statistical analyses used in the GLP-1 trial and aims to minimize bias and data-driven reporting of results. TRIAL REGISTRATION: 1) Danish National Board of Health, EudraCT 2013-004311-45. Registered on 25 March 2014. 2) Videnskabsetisk komité C, Region Hovedstaden, No. 45728. Registered on 29 January 2014. 3) Clinicaltrial.gov, NCT02442791. Registered on 25 of January 2015. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13063-016-1421-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-30 /pmc/articles/PMC4929765/ /pubmed/27363489 http://dx.doi.org/10.1186/s13063-016-1421-2 Text en © Wiberg et al. 2016 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.
spellingShingle Study Protocol
Wiberg, Sebastian
Hassager, Christian
Thomsen, Jakob Hartvig
Frydland, Martin
Høfsten, Dan Eik
Engstrøm, Thomas
Køber, Lars
Schmidt, Henrik
Møller, Jacob Eifer
Kjaergaard, Jesper
GLP-1 analogues for neuroprotection after out-of-hospital cardiac arrest: study protocol for a randomized controlled trial
title GLP-1 analogues for neuroprotection after out-of-hospital cardiac arrest: study protocol for a randomized controlled trial
title_full GLP-1 analogues for neuroprotection after out-of-hospital cardiac arrest: study protocol for a randomized controlled trial
title_fullStr GLP-1 analogues for neuroprotection after out-of-hospital cardiac arrest: study protocol for a randomized controlled trial
title_full_unstemmed GLP-1 analogues for neuroprotection after out-of-hospital cardiac arrest: study protocol for a randomized controlled trial
title_short GLP-1 analogues for neuroprotection after out-of-hospital cardiac arrest: study protocol for a randomized controlled trial
title_sort glp-1 analogues for neuroprotection after out-of-hospital cardiac arrest: study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4929765/
https://www.ncbi.nlm.nih.gov/pubmed/27363489
http://dx.doi.org/10.1186/s13063-016-1421-2
work_keys_str_mv AT wibergsebastian glp1analoguesforneuroprotectionafteroutofhospitalcardiacarreststudyprotocolforarandomizedcontrolledtrial
AT hassagerchristian glp1analoguesforneuroprotectionafteroutofhospitalcardiacarreststudyprotocolforarandomizedcontrolledtrial
AT thomsenjakobhartvig glp1analoguesforneuroprotectionafteroutofhospitalcardiacarreststudyprotocolforarandomizedcontrolledtrial
AT frydlandmartin glp1analoguesforneuroprotectionafteroutofhospitalcardiacarreststudyprotocolforarandomizedcontrolledtrial
AT høfstendaneik glp1analoguesforneuroprotectionafteroutofhospitalcardiacarreststudyprotocolforarandomizedcontrolledtrial
AT engstrømthomas glp1analoguesforneuroprotectionafteroutofhospitalcardiacarreststudyprotocolforarandomizedcontrolledtrial
AT køberlars glp1analoguesforneuroprotectionafteroutofhospitalcardiacarreststudyprotocolforarandomizedcontrolledtrial
AT schmidthenrik glp1analoguesforneuroprotectionafteroutofhospitalcardiacarreststudyprotocolforarandomizedcontrolledtrial
AT møllerjacobeifer glp1analoguesforneuroprotectionafteroutofhospitalcardiacarreststudyprotocolforarandomizedcontrolledtrial
AT kjaergaardjesper glp1analoguesforneuroprotectionafteroutofhospitalcardiacarreststudyprotocolforarandomizedcontrolledtrial