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Statistical analysis plan for the Erythropoietin in Traumatic Brain Injury trial: a randomised controlled trial of erythropoietin versus placebo in moderate and severe traumatic brain injury

Identifieur interne : 003501 ( Main/Exploration ); précédent : 003500; suivant : 003502

Statistical analysis plan for the Erythropoietin in Traumatic Brain Injury trial: a randomised controlled trial of erythropoietin versus placebo in moderate and severe traumatic brain injury

Auteurs : Jeffrey Presneill [Australie] ; Lorraine Little [Australie] ; Alistair Nichol [Australie, Irlande (pays)] ; Craig French [Australie] ; D James Cooper [Australie] ; Samir Haddad [Australie] ; Jacques Duranteau [Australie] ; Olivier Huet [France] ; Markus Skrifvars ; Yaseen Arabi [Australie] ; Rinaldo Bellomo [Australie]

Source :

RBID : PMC:4414377

Descripteurs français

English descriptors

Abstract

Background

The Erythropoietin in Traumatic Brain Injury (EPO-TBI) trial aims to determine whether the administration of erythropoietin to patients with moderate or severe traumatic brain injury improves patient-centred outcomes.

Methods

EPO-TBI is a multicentre, blinded, randomised, parallel groups, placebo-controlled, phase III superiority trial of erythropoietin in ICU patients with traumatic brain injury conducted in Australia and New Zealand, Saudi Arabia and Europe; 606 critically ill patients aged 15 to 65 years with moderate or severe acute traumatic brain injury will be enrolled.

Trial patients will receive either 40,000 IU erythropoietin or placebo by subcutaneous injection administered weekly for up to three doses during their ICU admission.

The primary outcome measure is the proportion of unfavourable neurological outcomes, comprising death or severe disability, observed at 6 months following randomisation utilizing the Extended Glasgow Outcome Scale. Secondary outcomes, also assessed at 6 months following randomisation, include the probability of an equal or greater Extended Glasgow Outcome Scale level, mortality, the proportions of patients with proximal deep venous thrombosis or with composite thrombotic vascular events, as well as assessment of quality of life and cost-effectiveness. The planned sample size will allow 90% power to detect a reduction from 50% to 36% in unfavourable neurological outcomes at a two-sided alpha of 0.05.

Discussion

A detailed analysis plan has been developed for EPO-TBI that is consistent with international guidelines. This plan specifies the statistical models for evaluation of primary and secondary outcomes, as well as defining covariates for adjusted analyses.

Application of this statistical analysis plan to the forthcoming EPO-TBI trial will facilitate unbiased analyses of these important clinical data.

Trial registration

Australian New Zealand Clinical Trials Registry: ACTRN12609000827235 (22 September 2009). ClinicalTrials.gov: NCT00987454 (29 September 2009). European Drug Regulatory Authorities Clinical Trials: 2011-005235-22 (18 January 2012).

Electronic supplementary material

The online version of this article (doi:10.1186/1745-6215-15-501) contains supplementary material, which is available to authorized users.


Url:
DOI: 10.1186/1745-6215-15-501
PubMed: 25528574
PubMed Central: 4414377


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<name sortKey="Skrifvars, Markus" sort="Skrifvars, Markus" uniqKey="Skrifvars M" first="Markus" last="Skrifvars">Markus Skrifvars</name>
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<name sortKey="Arabi, Yaseen" sort="Arabi, Yaseen" uniqKey="Arabi Y" first="Yaseen" last="Arabi">Yaseen Arabi</name>
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<nlm:aff id="Aff96">Intensive Care Department, College of Medicine King Saud Bin Abdulaziz University for Health Sciences and King Abdullah International Medical Research Center, PO Box 22490, Riyadh, 11426 Kingdom of Saudi Arabia</nlm:aff>
<wicri:noCountry code="subfield">11426 Kingdom of Saudi Arabia</wicri:noCountry>
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<name sortKey="Bellomo, Rinaldo" sort="Bellomo, Rinaldo" uniqKey="Bellomo R" first="Rinaldo" last="Bellomo">Rinaldo Bellomo</name>
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<nlm:aff id="Aff91">The University of Melbourne, Grattan Street, Parkville, 3052 Australia</nlm:aff>
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<nlm:aff id="Aff97">Department of Intensive Care, Austin Health, Studley Road, Heidelberg, 3084 Australia</nlm:aff>
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<series>
<title level="j">Trials</title>
<idno type="eISSN">1745-6215</idno>
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<date when="2014">2014</date>
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<term>Adolescent</term>
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<term>Aged</term>
<term>Australia</term>
<term>Brain Injuries (diagnosis)</term>
<term>Brain Injuries (drug therapy)</term>
<term>Brain Injuries (economics)</term>
<term>Brain Injuries (mortality)</term>
<term>Clinical Protocols</term>
<term>Cost-Benefit Analysis</term>
<term>Critical Illness</term>
<term>Data Interpretation, Statistical</term>
<term>Disability Evaluation</term>
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<term>Erythropoietin (administration & dosage)</term>
<term>Erythropoietin (adverse effects)</term>
<term>Erythropoietin (economics)</term>
<term>Europe</term>
<term>Female</term>
<term>Humans</term>
<term>Injections, Subcutaneous</term>
<term>Injury Severity Score</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Models, Statistical</term>
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<term>Prospective Studies</term>
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<term>Adolescent</term>
<term>Adulte</term>
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<term>Analyse coût-bénéfice</term>
<term>Arabie saoudite</term>
<term>Australie</term>
<term>Calendrier d'administration des médicaments</term>
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<term>Qualité de vie</term>
<term>Récupération fonctionnelle</term>
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<term>Neuroprotective Agents</term>
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<term>Lésions encéphaliques</term>
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<term>Brain Injuries</term>
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<term>Injections sous-cutanées</term>
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<front>
<div type="abstract" xml:lang="en">
<sec>
<title>Background</title>
<p>The Erythropoietin in Traumatic Brain Injury (EPO-TBI) trial aims to determine whether the administration of erythropoietin to patients with moderate or severe traumatic brain injury improves patient-centred outcomes.</p>
</sec>
<sec>
<title>Methods</title>
<p>EPO-TBI is a multicentre, blinded, randomised, parallel groups, placebo-controlled, phase III superiority trial of erythropoietin in ICU patients with traumatic brain injury conducted in Australia and New Zealand, Saudi Arabia and Europe; 606 critically ill patients aged 15 to 65 years with moderate or severe acute traumatic brain injury will be enrolled.</p>
<p>Trial patients will receive either 40,000 IU erythropoietin or placebo by subcutaneous injection administered weekly for up to three doses during their ICU admission.</p>
<p>The primary outcome measure is the proportion of unfavourable neurological outcomes, comprising death or severe disability, observed at 6 months following randomisation utilizing the Extended Glasgow Outcome Scale. Secondary outcomes, also assessed at 6 months following randomisation, include the probability of an equal or greater Extended Glasgow Outcome Scale level, mortality, the proportions of patients with proximal deep venous thrombosis or with composite thrombotic vascular events, as well as assessment of quality of life and cost-effectiveness. The planned sample size will allow 90% power to detect a reduction from 50% to 36% in unfavourable neurological outcomes at a two-sided alpha of 0.05.</p>
</sec>
<sec>
<title>Discussion</title>
<p>A detailed analysis plan has been developed for EPO-TBI that is consistent with international guidelines. This plan specifies the statistical models for evaluation of primary and secondary outcomes, as well as defining covariates for adjusted analyses.</p>
<p>Application of this statistical analysis plan to the forthcoming EPO-TBI trial will facilitate unbiased analyses of these important clinical data.</p>
</sec>
<sec>
<title>Trial registration</title>
<p>Australian New Zealand Clinical Trials Registry:
<ext-link ext-link-type="uri" xlink:href="http://www.anzctr.org.au/ACTRN12609000827235">ACTRN12609000827235</ext-link>
(22 September 2009). ClinicalTrials.gov:
<ext-link ext-link-type="uri" xlink:href="http://www.anzctr.org.au/">NCT00987454</ext-link>
(29 September 2009). European Drug Regulatory Authorities Clinical Trials: 2011-005235-22 (18 January 2012).</p>
</sec>
<sec>
<title>Electronic supplementary material</title>
<p>The online version of this article (doi:10.1186/1745-6215-15-501) contains supplementary material, which is available to authorized users.</p>
</sec>
</div>
</front>
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</div1>
</back>
</TEI>
<affiliations>
<list>
<country>
<li>Australie</li>
<li>France</li>
<li>Irlande (pays)</li>
</country>
<region>
<li>Victoria (État)</li>
</region>
<settlement>
<li>Melbourne</li>
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<orgName>
<li>Université de Melbourne</li>
</orgName>
</list>
<tree>
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<name sortKey="Skrifvars, Markus" sort="Skrifvars, Markus" uniqKey="Skrifvars M" first="Markus" last="Skrifvars">Markus Skrifvars</name>
</noCountry>
<country name="Australie">
<region name="Victoria (État)">
<name sortKey="Presneill, Jeffrey" sort="Presneill, Jeffrey" uniqKey="Presneill J" first="Jeffrey" last="Presneill">Jeffrey Presneill</name>
</region>
<name sortKey="Arabi, Yaseen" sort="Arabi, Yaseen" uniqKey="Arabi Y" first="Yaseen" last="Arabi">Yaseen Arabi</name>
<name sortKey="Bellomo, Rinaldo" sort="Bellomo, Rinaldo" uniqKey="Bellomo R" first="Rinaldo" last="Bellomo">Rinaldo Bellomo</name>
<name sortKey="Bellomo, Rinaldo" sort="Bellomo, Rinaldo" uniqKey="Bellomo R" first="Rinaldo" last="Bellomo">Rinaldo Bellomo</name>
<name sortKey="Bellomo, Rinaldo" sort="Bellomo, Rinaldo" uniqKey="Bellomo R" first="Rinaldo" last="Bellomo">Rinaldo Bellomo</name>
<name sortKey="Cooper, D James" sort="Cooper, D James" uniqKey="Cooper D" first="D James" last="Cooper">D James Cooper</name>
<name sortKey="Cooper, D James" sort="Cooper, D James" uniqKey="Cooper D" first="D James" last="Cooper">D James Cooper</name>
<name sortKey="Duranteau, Jacques" sort="Duranteau, Jacques" uniqKey="Duranteau J" first="Jacques" last="Duranteau">Jacques Duranteau</name>
<name sortKey="French, Craig" sort="French, Craig" uniqKey="French C" first="Craig" last="French">Craig French</name>
<name sortKey="French, Craig" sort="French, Craig" uniqKey="French C" first="Craig" last="French">Craig French</name>
<name sortKey="Haddad, Samir" sort="Haddad, Samir" uniqKey="Haddad S" first="Samir" last="Haddad">Samir Haddad</name>
<name sortKey="Little, Lorraine" sort="Little, Lorraine" uniqKey="Little L" first="Lorraine" last="Little">Lorraine Little</name>
<name sortKey="Nichol, Alistair" sort="Nichol, Alistair" uniqKey="Nichol A" first="Alistair" last="Nichol">Alistair Nichol</name>
<name sortKey="Nichol, Alistair" sort="Nichol, Alistair" uniqKey="Nichol A" first="Alistair" last="Nichol">Alistair Nichol</name>
<name sortKey="Presneill, Jeffrey" sort="Presneill, Jeffrey" uniqKey="Presneill J" first="Jeffrey" last="Presneill">Jeffrey Presneill</name>
</country>
<country name="Irlande (pays)">
<noRegion>
<name sortKey="Nichol, Alistair" sort="Nichol, Alistair" uniqKey="Nichol A" first="Alistair" last="Nichol">Alistair Nichol</name>
</noRegion>
<name sortKey="Nichol, Alistair" sort="Nichol, Alistair" uniqKey="Nichol A" first="Alistair" last="Nichol">Alistair Nichol</name>
</country>
<country name="France">
<noRegion>
<name sortKey="Huet, Olivier" sort="Huet, Olivier" uniqKey="Huet O" first="Olivier" last="Huet">Olivier Huet</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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