Cargando…
Determining the Feasibility of Ambulance-Based Randomised Controlled Trials in Patients with Ultra-Acute Stroke: Study Protocol for the “Rapid Intervention with GTN in Hypertensive Stroke Trial” (RIGHT, ISRCTN66434824)
Background. Time from acute stroke to enrolment in clinical trials needs to be reduced to improve the chances of finding effective treatments. No completed randomised controlled trials of ambulance-based treatment for acute stroke have been reported in the UK, and the practicalities of recruiting, c...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480012/ https://www.ncbi.nlm.nih.gov/pubmed/23125943 http://dx.doi.org/10.1155/2012/385753 |
_version_ | 1782247497269248000 |
---|---|
author | Ankolekar, Sandeep Sare, Gillian Geeganage, Chamila Fuller, Michael Stokes, Lynn Sprigg, Nikola Parry, Ruth Siriwardena, A. Niroshan Bath, Philip M. W. |
author_facet | Ankolekar, Sandeep Sare, Gillian Geeganage, Chamila Fuller, Michael Stokes, Lynn Sprigg, Nikola Parry, Ruth Siriwardena, A. Niroshan Bath, Philip M. W. |
author_sort | Ankolekar, Sandeep |
collection | PubMed |
description | Background. Time from acute stroke to enrolment in clinical trials needs to be reduced to improve the chances of finding effective treatments. No completed randomised controlled trials of ambulance-based treatment for acute stroke have been reported in the UK, and the practicalities of recruiting, consenting, and treating patients are unknown. Methods. RIGHT is an ambulance based, single-blind, randomised controlled trial with blinded-outcome assessment. The trial will assess feasibility of using ambulance services to deliver ultra-acute stroke treatments; a secondary aim is to assess the effect of glyceryl trinitrate (GTN) on haemodynamic variables and functional outcomes. Initial consent, randomisation, and treatment are performed by paramedics prior to hospitalisation. Patients with ultra-acute stroke (≤4 hours of onset) are randomised to transdermal GTN (5 mg/24 hours) or gauze dressing daily for 7 days. The primary outcome is systolic blood pressure at 2 hours. Secondary outcomes include feasibility, haemodynamics, dependency, and other functional outcomes. A nested qualitative study is included. Trial Status. The trial has all relevant ethics and regulatory approvals and recruitment started on February 15, 2010. The trial stopped recruitment in December 2011 after 41 patients were recruited. Trial Registration. The trial registration number is ISRCTN66434824 and EudraCT number is 2007-004766-40. |
format | Online Article Text |
id | pubmed-3480012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-34800122012-11-02 Determining the Feasibility of Ambulance-Based Randomised Controlled Trials in Patients with Ultra-Acute Stroke: Study Protocol for the “Rapid Intervention with GTN in Hypertensive Stroke Trial” (RIGHT, ISRCTN66434824) Ankolekar, Sandeep Sare, Gillian Geeganage, Chamila Fuller, Michael Stokes, Lynn Sprigg, Nikola Parry, Ruth Siriwardena, A. Niroshan Bath, Philip M. W. Stroke Res Treat Clinical Study Background. Time from acute stroke to enrolment in clinical trials needs to be reduced to improve the chances of finding effective treatments. No completed randomised controlled trials of ambulance-based treatment for acute stroke have been reported in the UK, and the practicalities of recruiting, consenting, and treating patients are unknown. Methods. RIGHT is an ambulance based, single-blind, randomised controlled trial with blinded-outcome assessment. The trial will assess feasibility of using ambulance services to deliver ultra-acute stroke treatments; a secondary aim is to assess the effect of glyceryl trinitrate (GTN) on haemodynamic variables and functional outcomes. Initial consent, randomisation, and treatment are performed by paramedics prior to hospitalisation. Patients with ultra-acute stroke (≤4 hours of onset) are randomised to transdermal GTN (5 mg/24 hours) or gauze dressing daily for 7 days. The primary outcome is systolic blood pressure at 2 hours. Secondary outcomes include feasibility, haemodynamics, dependency, and other functional outcomes. A nested qualitative study is included. Trial Status. The trial has all relevant ethics and regulatory approvals and recruitment started on February 15, 2010. The trial stopped recruitment in December 2011 after 41 patients were recruited. Trial Registration. The trial registration number is ISRCTN66434824 and EudraCT number is 2007-004766-40. Hindawi Publishing Corporation 2012 2012-10-16 /pmc/articles/PMC3480012/ /pubmed/23125943 http://dx.doi.org/10.1155/2012/385753 Text en Copyright © 2012 Sandeep Ankolekar et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Study Ankolekar, Sandeep Sare, Gillian Geeganage, Chamila Fuller, Michael Stokes, Lynn Sprigg, Nikola Parry, Ruth Siriwardena, A. Niroshan Bath, Philip M. W. Determining the Feasibility of Ambulance-Based Randomised Controlled Trials in Patients with Ultra-Acute Stroke: Study Protocol for the “Rapid Intervention with GTN in Hypertensive Stroke Trial” (RIGHT, ISRCTN66434824) |
title | Determining the Feasibility of Ambulance-Based Randomised Controlled Trials in Patients with Ultra-Acute Stroke: Study Protocol for the “Rapid Intervention with GTN in Hypertensive Stroke Trial” (RIGHT, ISRCTN66434824) |
title_full | Determining the Feasibility of Ambulance-Based Randomised Controlled Trials in Patients with Ultra-Acute Stroke: Study Protocol for the “Rapid Intervention with GTN in Hypertensive Stroke Trial” (RIGHT, ISRCTN66434824) |
title_fullStr | Determining the Feasibility of Ambulance-Based Randomised Controlled Trials in Patients with Ultra-Acute Stroke: Study Protocol for the “Rapid Intervention with GTN in Hypertensive Stroke Trial” (RIGHT, ISRCTN66434824) |
title_full_unstemmed | Determining the Feasibility of Ambulance-Based Randomised Controlled Trials in Patients with Ultra-Acute Stroke: Study Protocol for the “Rapid Intervention with GTN in Hypertensive Stroke Trial” (RIGHT, ISRCTN66434824) |
title_short | Determining the Feasibility of Ambulance-Based Randomised Controlled Trials in Patients with Ultra-Acute Stroke: Study Protocol for the “Rapid Intervention with GTN in Hypertensive Stroke Trial” (RIGHT, ISRCTN66434824) |
title_sort | determining the feasibility of ambulance-based randomised controlled trials in patients with ultra-acute stroke: study protocol for the “rapid intervention with gtn in hypertensive stroke trial” (right, isrctn66434824) |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3480012/ https://www.ncbi.nlm.nih.gov/pubmed/23125943 http://dx.doi.org/10.1155/2012/385753 |
work_keys_str_mv | AT ankolekarsandeep determiningthefeasibilityofambulancebasedrandomisedcontrolledtrialsinpatientswithultraacutestrokestudyprotocolfortherapidinterventionwithgtninhypertensivestroketrialrightisrctn66434824 AT saregillian determiningthefeasibilityofambulancebasedrandomisedcontrolledtrialsinpatientswithultraacutestrokestudyprotocolfortherapidinterventionwithgtninhypertensivestroketrialrightisrctn66434824 AT geeganagechamila determiningthefeasibilityofambulancebasedrandomisedcontrolledtrialsinpatientswithultraacutestrokestudyprotocolfortherapidinterventionwithgtninhypertensivestroketrialrightisrctn66434824 AT fullermichael determiningthefeasibilityofambulancebasedrandomisedcontrolledtrialsinpatientswithultraacutestrokestudyprotocolfortherapidinterventionwithgtninhypertensivestroketrialrightisrctn66434824 AT stokeslynn determiningthefeasibilityofambulancebasedrandomisedcontrolledtrialsinpatientswithultraacutestrokestudyprotocolfortherapidinterventionwithgtninhypertensivestroketrialrightisrctn66434824 AT spriggnikola determiningthefeasibilityofambulancebasedrandomisedcontrolledtrialsinpatientswithultraacutestrokestudyprotocolfortherapidinterventionwithgtninhypertensivestroketrialrightisrctn66434824 AT parryruth determiningthefeasibilityofambulancebasedrandomisedcontrolledtrialsinpatientswithultraacutestrokestudyprotocolfortherapidinterventionwithgtninhypertensivestroketrialrightisrctn66434824 AT siriwardenaaniroshan determiningthefeasibilityofambulancebasedrandomisedcontrolledtrialsinpatientswithultraacutestrokestudyprotocolfortherapidinterventionwithgtninhypertensivestroketrialrightisrctn66434824 AT bathphilipmw determiningthefeasibilityofambulancebasedrandomisedcontrolledtrialsinpatientswithultraacutestrokestudyprotocolfortherapidinterventionwithgtninhypertensivestroketrialrightisrctn66434824 |