Evidence map›Paper›PMID 31587658›Full record

Trial reportStroke2019

Prehospital Transdermal Glyceryl Trinitrate for Ultra-Acute Intracerebral Hemorrhage: Data From the RIGHT-2 Trial.

Philip M Bath, Lisa J Woodhouse, Kailash Krishnan, Jason P Appleton, Craig S Anderson, Eivind Berge, Lesley Cala, Mark Dixon, Timothy J England, Peter J Godolphin and 17 more

Open access · greenAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Stroke, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 6 pooled it
6.0field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

37 citing papers in PubMed, 6 syntheses or guidelines pooled it, 69 citations in OpenAlex.

  1. Pooled it
  2. Guideline
  3. Pooled it
  4. Pooled it
  5. Therapeutic Variation in Lowering Blood Pressure: Effects on Intracranial Pressure in Acute Intracerebral Haemorrhage.High blood pressure & cardiovascular prevention : the official journal of the Italian Society of Hypertension · 2021
    Pooled it
  6. Pooled it
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Review
  13. Review
  14. Review
  15. Linking Triglyceride-Glucose Index to Spontaneous Intracerebral Hemorrhage: Mechanisms and Predictive Insights.Medical science monitor : international medical journal of experimental and clinical research · 2025
    Review
  16. Review
  17. Extracellular Vesicles as a Potential Therapy for Stroke.International journal of molecular sciences · 2025
    Review
  18. The hazards of chasing subgroups in neutral stroke trials.Neurological research and practice · 2025
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors at 17 institutions in 6 countries.

Philip M BathFrom the Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, United Kingdom (P.M.B., L.J.W., J.P.A., M.D., N.S.).
Lisa J WoodhouseFrom the Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, United Kingdom (P.M.B., L.J.W., J.P.A., M.D., N.S.).
Kailash KrishnanStroke, Nottingham University Hospitals National Health Service (NHS) Trust, City Hospital Campus, United Kingdom (P.M.B., K.K., N.S.).
Jason P AppletonFrom the Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, United Kingdom (P.M.B., L.J.W., J.P.A., M.D., N.S.).
Craig S AndersonThe George Institute for Global Health, Faculty of Medicine, University of New South Wales, Sydney, Australia (C.S.A.).
Eivind BergeDepartment of Internal Medicine (E.B., A.N.S), Oslo University Hospital, Norway.
Lesley CalaFaculty of Health and Medical Sciences, University of Western Australia (L.C.).
Mark DixonFrom the Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, United Kingdom (P.M.B., L.J.W., J.P.A., M.D., N.S.).
Timothy J EnglandVascular Medicine, Division of Medical Sciences, GEM, Royal Derby Hospital Centre (T.J.E.), University of Nottingham, United Kingdom.
Peter J GodolphinNottingham Clinical Trials Unit, Queen's Medical Centre (P.J.G., T.H., A.A.M.), University of Nottingham, United Kingdom.
Trish HepburnNottingham Clinical Trials Unit, Queen's Medical Centre (P.J.G., T.H., A.A.M.), University of Nottingham, United Kingdom.
Grant MairCentre for Clinical Brain Sciences, Edinburgh Imaging and UK Dementia Research Institute at the University of Edinburgh, Chancellor's Building (G.M., J.M.W.).
Alan A MontgomeryNottingham Clinical Trials Unit, Queen's Medical Centre (P.J.G., T.H., A.A.M.), University of Nottingham, United Kingdom.
Stephen J PhillipsDepartment of Medicine, Dalhousie University and Queen Elizabeth II Health Sciences Centre, Halifax, Canada (S.J.P.).
John PotterBob Champion Research and Education Building, University of East Anglia, Norwich, United Kingdom (J.P.).
Chris I PriceInstitute of Neuroscience, Newcastle University, United Kingdom (C.I.P.).
Marc RandallDepartment of Neurology, Leeds Teaching Hospitals NHS Trust, United Kingdom (M.R.).
Thompson G RobinsonDepartment of Cardiovascular Sciences and NIHR Leicester Biomedical Research Centre, University of Leicester, United Kingdom (T.G.R.).
Christine RoffeStroke Research in Stoke, Institute for Science and Technology in Medicine, Keele University, Stoke-on-Trent, United Kingdom (C.R.).
Peter M RothwellNuffield Department of Clinical Neurosciences, John Radcliffe Hospital, Oxford, United Kingdom (P.M.R.).
Else C SandsetResearch and Development, The Norwegian Air Ambulance Foundation, Oslo, Norway (E.C.S.).
Nerses SanossianDepartment of Neurology, University of Southern California Keck School of Medicine, Los Angeles (N.S.).
Jeffrey L SaverDepartment of Neurology and Comprehensive Stroke Center, David Geffen School of Medicine at UCLA (J.L.S.).
A Niroshan SiriwardenaDepartment of Internal Medicine (E.B., A.N.S), Oslo University Hospital, Norway.
Graham VenablesDepartment of Neurology, Royal Hallamshire Hospital, Sheffield, United Kingdom (G.V.).
Joanna M WardlawCentre for Clinical Brain Sciences, Edinburgh Imaging and UK Dementia Research Institute at the University of Edinburgh, Chancellor's Building (G.M., J.M.W.).
Nikola SpriggFrom the Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, United Kingdom (P.M.B., L.J.W., J.P.A., M.D., N.S.).
University of Nottingham · GBOslo University Hospital · NOQueen's Medical Centre · GBUK Dementia Research Institute · GBGeorge Institute for Global Health · CNJohn Radcliffe Hospital · GBKeele University · GBLeeds Teaching Hospitals NHS Trust · GBNational Health Service · GBNewcastle University · GBNIHR Leicester Biomedical Research Centre · GBQueen Elizabeth II Health Sciences Centre · CARoyal Derby Hospital · GBStiftelsen Norsk Luftambulanse · NOUniversity of East Anglia · GBUniversity of Southern California · USUniversity of Western Australia · AU

Funding

British Heart Foundation CS/14/4/30972
6 · The paper itself

Abstract

Background and Purpose- Pilot trials suggest that glyceryl trinitrate (GTN; nitroglycerin) may improve outcome when administered early after stroke onset. Methods- We undertook a multicentre, paramedic-delivered, ambulance-based, prospective randomized, sham-controlled, blinded-end point trial in adults with presumed stroke within 4 hours of ictus. Participants received transdermal GTN (5 mg) or a sham dressing (1:1) in the ambulance and then daily for three days in hospital. The primary outcome was the 7-level modified Rankin Scale at 90 days assessed by central telephone treatment-blinded follow-up. This prespecified subgroup analysis focuses on participants with an intracerebral hemorrhage as their index event. Analyses are intention-to-treat. Results- Of 1149 participants with presumed stroke, 145 (13%; GTN, 74; sham, 71) had an intracerebral hemorrhage: time from onset to randomization median, 74 minutes (interquartile range, 45-110). By admission to hospital, blood pressure tended to be lower with GTN as compared with sham: mean, 4.4/3.5 mm Hg. The modified Rankin Scale score at 90 days was nonsignificantly higher in the GTN group: adjusted common odds ratio for poor outcome, 1.87 (95% CI, 0.98-3.57). A prespecified global analysis of 5 clinical outcomes (dependency, disability, cognition, quality of life, and mood) was worse with GTN; Mann-Whitney difference, 0.18 (95% CI, 0.01-0.35; Wei-Lachin test). GTN was associated with larger hematoma and growth, and more mass effect and midline shift on neuroimaging, and altered use of hospital resources. Death in hospital but not at day 90 was increased with GTN. There were no significant between-group differences in serious adverse events. Conclusions- Prehospital treatment with GTN worsened outcomes in patients with intracerebral hemorrhage. Since these results could relate to the play of chance, confounding, or a true effect of GTN, further randomized evidence on the use of vasodilators in ultra-acute intracerebral hemorrhage is needed. Clinical Trial Registration- URL: http://www.controlled-trials.com. Unique identifier: ISRCTN26986053.

Indexed as

Cerebral HemorrhageEmergency Medical ServicesHospital MortalityNitroglycerinStrokeAcute DiseaseAdministration, CutaneousAgedAged, 80 and overBlood PressureFemaleHumansMaleMiddle AgedProspective StudiesTime FactorsNitroglycerinallied health personnelambulancesblood pressurehumansnitroglycerin

Identifiers

PMID31587658
PMCPMC6824503
OpenAlexW2980000583

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.