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Intravenous tranexamic acid for hyperacute primary intracerebral hemorrhage: protocol for a randomized, placebo-controlled trial

Sprigg, Nikola; Robson, Katie; Bath, Philip M.W.; Dineen, Robert A.; Roberts, Ian; Robinson, Tom; Roffe, Christine; Werring, David; Al-Shahi Salman, Rustam; Pocock, Stuart J.; Duley, Lelia; England, Timothy J.; Whynes, David; Ciccone, Alfonso; Laska, Ann Charlotte; Christensen, Hanne; Ozturk, Serefnur; Collins, Ronan; Bereczki, Daniel; Egea-Guerrero, Juan Jose; Law, Zhe Kang; Czlonkowska, Anna; Seiffge, David; Beredzie, Maia

Authors

NIKOLA SPRIGG nikola.sprigg@nottingham.ac.uk
Professor of Stroke Medicine

Katie Robson

Philip M.W. Bath

Robert A. Dineen

Ian Roberts

Tom Robinson

Christine Roffe

David Werring

Rustam Al-Shahi Salman

Stuart J. Pocock

Lelia Duley

Timothy J. England

David Whynes

Alfonso Ciccone

Ann Charlotte Laska

Hanne Christensen

Serefnur Ozturk

Ronan Collins

Daniel Bereczki

Juan Jose Egea-Guerrero

Zhe Kang Law

Anna Czlonkowska

David Seiffge

Maia Beredzie



Abstract

Rationale: Outcome after intracerebral hemorrhage remains poor. Tranexamic acid is easy to administer, readily available, inexpensive, and effective in other hemorrhagic conditions.

Aim: This randomized trial aims to test the hypothesis that intravenous tranexamic acid given within 8?h of spontaneous intracerebral hemorrhage reduces death or dependency.

Design: Phase III prospective double-blind randomized placebo-controlled trial. Participants within 8?h of spontaneous intracerebral hemorrhage are randomized to receive either intravenous tranexamic acid 1?g 10?min bolus followed by 1?g 8?h infusion, or placebo.

Sample size estimates: A trial of 2000 participants (300 from start-up phase and 1700 from main phase) will have 90% power to detect an ordinal shift of the modified Rankin Scale with odds ratio 0.79.

Study outcomes: The primary outcome is death or dependency measured by ordinal shift analysis of the 7 level mRS at day 90. Secondary outcomes are neurological impairment at day 7 and disability, quality of life, cognition, and mood at day 90. Safety outcomes are death, serious adverse events, thromboembolic events, and seizures. Cost outcomes are length of stay in hospital, readmission, and institutionalization.

Discussion: This pragmatic trial is assessing efficacy of tranexamic acid after spontaneous intracerebral hemorrhage. Recruitment started in 2013; as of 15th January 2016 1355 participants have been enrolled, from 95 centers in seven countries. Recruitment is due to end in 2017. TICH-2 Trial is registered as ISRCTN93732214.

Citation

Sprigg, N., Robson, K., Bath, P. M., Dineen, R. A., Roberts, I., Robinson, T., …Beredzie, M. (2016). Intravenous tranexamic acid for hyperacute primary intracerebral hemorrhage: protocol for a randomized, placebo-controlled trial. International Journal of Stroke, 11(6), https://doi.org/10.1177/1747493016641960

Journal Article Type Article
Acceptance Date Feb 14, 2016
Online Publication Date Apr 5, 2016
Publication Date Aug 1, 2016
Deposit Date Aug 4, 2016
Journal International Journal of Stroke
Print ISSN 1747-4930
Electronic ISSN 1747-4949
Publisher SAGE Publications
Peer Reviewed Peer Reviewed
Volume 11
Issue 6
DOI https://doi.org/10.1177/1747493016641960
Keywords Hyperacute intracerebral hemorrhage, tranexamic acid, randomized trial, placebo controlled
Public URL https://nottingham-repository.worktribe.com/output/975644
Publisher URL http://wso.sagepub.com/content/11/6/683.1