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Multicentre Randomised trial of Acute Stroke treatment in the Ambulance with a nitroglycerin Patch (MR ASAP): study protocol for a randomised controlled trial

Authors :
van den Berg, S.A. (Sophie A.)
Dippel, D.W.J. (Diederik)
Hofmeijer, J.
Fransen, P.S.S. (Puck)
Caminada, K. (Klaartje)
Siegers, A. (Arjen)
Kruyt, N.D. (Nyika)
Kerkhoff, H. (Henk)
Leeuw, H.F. (Frank) de
Nederkoorn, P.J. (Paul)
Worp, H.B. (Bart) van der
van den Berg, S.A. (Sophie A.)
Dippel, D.W.J. (Diederik)
Hofmeijer, J.
Fransen, P.S.S. (Puck)
Caminada, K. (Klaartje)
Siegers, A. (Arjen)
Kruyt, N.D. (Nyika)
Kerkhoff, H. (Henk)
Leeuw, H.F. (Frank) de
Nederkoorn, P.J. (Paul)
Worp, H.B. (Bart) van der
Publication Year :
2019

Abstract

BACKGROUND: Some studies have suggested that transdermal administration of glyceryl trinitrate (GTN; nitroglycerin) in the first few hours after symptom onset increases the chance of a favourable outcome after ischaemic stroke or intracerebral haemorrhage, possibly through an increase in intracranial collateral blood flow and a reduction in blood pressure. The Multicentre Randomised trial of Acute Stroke treatment in the Ambulance with a nitroglycerin Patch (MR ASAP) aims to assess the effect of transdermal GTN, started within 3 h after stroke onset in the prehospital setting, on functional outcome at 90 days in patients with acute ischaemic stroke or intracerebral haemorrhage. METHODS: MR ASAP is a phase III, multicentre, randomised, open-label clinical trial with a blinded outcome assessment. A total of 1400 adult patients with suspected stroke and a systolic blood pressure ≥ 140 mmHg will be randomised to transdermal GTN (5 mg/day), administered as a transdermal patch by paramedics in the prehospital setting within 3 h of stroke onset and continued for 24 h or to standard care. The primary outcome is the score on the modified Rankin Scale (mRS) at 90 days, analysed with ordinal logistic regression. Secondary outcomes include blood pressure and collateral circulation at hospital admission, neurological deficit measured with the National Institutes of Health Stroke Scale at 24 h, and mortality and poor outcome (mRS score 3 to 6) at 90 days. This trial will be conducted in the Netherlands and will use a deferred consent procedure. The trial is part of the Collaboration for New Treatments of Acute Stro

Details

Database :
OAIster
Notes :
application/pdf, Trials vol. 20 no. 1, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1111585981
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1186.s13063-019-3419-z