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PRECISE - pregabalin in addition to usual care for sciatica: study protocol for a randomised controlled trial

BACKGROUND: Sciatica is a type of neuropathic pain that is characterised by pain radiating into the leg. It is often accompanied by low back pain and neurological deficits in the lower limb. While this condition may cause significant suffering for the individual, the lack of evidence supporting effe...

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Autores principales: Mathieson, Stephanie, Maher, Christopher G, McLachlan, Andrew J, Latimer, Jane, Koes, Bart W, Hancock, Mark J, Harris, Ian, Day, Richard O, Pik, Justin, Jan, Stephen, Billot, Laurent, Lin, Chung-Wei Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711833/
https://www.ncbi.nlm.nih.gov/pubmed/23845078
http://dx.doi.org/10.1186/1745-6215-14-213
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author Mathieson, Stephanie
Maher, Christopher G
McLachlan, Andrew J
Latimer, Jane
Koes, Bart W
Hancock, Mark J
Harris, Ian
Day, Richard O
Pik, Justin
Jan, Stephen
Billot, Laurent
Lin, Chung-Wei Christine
author_facet Mathieson, Stephanie
Maher, Christopher G
McLachlan, Andrew J
Latimer, Jane
Koes, Bart W
Hancock, Mark J
Harris, Ian
Day, Richard O
Pik, Justin
Jan, Stephen
Billot, Laurent
Lin, Chung-Wei Christine
author_sort Mathieson, Stephanie
collection PubMed
description BACKGROUND: Sciatica is a type of neuropathic pain that is characterised by pain radiating into the leg. It is often accompanied by low back pain and neurological deficits in the lower limb. While this condition may cause significant suffering for the individual, the lack of evidence supporting effective treatments for sciatica makes clinical management difficult. Our objectives are to determine the efficacy of pregabalin on reducing leg pain intensity and its cost-effectiveness in patients with sciatica. METHODS/DESIGN: PRECISE is a prospectively registered, double-blind, randomised placebo-controlled trial of pregabalin compared to placebo, in addition to usual care. Inclusion criteria include moderate to severe leg pain below the knee with evidence of nerve root/spinal nerve involvement. Participants will be randomised to receive either pregabalin with usual care (n = 102) or placebo with usual care (n = 102) for 8 weeks. The medicine dosage will be titrated up to the participant’s optimal dose, to a maximum 600 mg per day. Follow up consultations will monitor individual progress, tolerability and adverse events. Usual care, if deemed appropriate by the study doctor, may include a referral for physical or manual therapy and/or prescription of analgesic medication. Participants, doctors and researchers collecting participant data will be blinded to treatment allocation. Participants will be assessed at baseline and at weeks 2, 4, 8, 12, 26 and 52. The primary outcome will determine the efficacy of pregabalin in reducing leg pain intensity. Secondary outcomes will include back pain intensity, disability and quality of life. Data analysis will be blinded and by intention-to-treat. A parallel economic evaluation will be conducted from health sector and societal perspectives. DISCUSSION: This study will establish the efficacy of pregabalin in reducing leg pain intensity in patients with sciatica and provide important information regarding the effect of pregabalin treatment on disability and quality of life. The impact of this research may allow the future development of a cost-effective conservative treatment strategy for patients with sciatica. TRIAL REGISTRATION: ClinicalTrial.gov, ACTRN 12613000530729
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spelling pubmed-37118332013-07-16 PRECISE - pregabalin in addition to usual care for sciatica: study protocol for a randomised controlled trial Mathieson, Stephanie Maher, Christopher G McLachlan, Andrew J Latimer, Jane Koes, Bart W Hancock, Mark J Harris, Ian Day, Richard O Pik, Justin Jan, Stephen Billot, Laurent Lin, Chung-Wei Christine Trials Study Protocol BACKGROUND: Sciatica is a type of neuropathic pain that is characterised by pain radiating into the leg. It is often accompanied by low back pain and neurological deficits in the lower limb. While this condition may cause significant suffering for the individual, the lack of evidence supporting effective treatments for sciatica makes clinical management difficult. Our objectives are to determine the efficacy of pregabalin on reducing leg pain intensity and its cost-effectiveness in patients with sciatica. METHODS/DESIGN: PRECISE is a prospectively registered, double-blind, randomised placebo-controlled trial of pregabalin compared to placebo, in addition to usual care. Inclusion criteria include moderate to severe leg pain below the knee with evidence of nerve root/spinal nerve involvement. Participants will be randomised to receive either pregabalin with usual care (n = 102) or placebo with usual care (n = 102) for 8 weeks. The medicine dosage will be titrated up to the participant’s optimal dose, to a maximum 600 mg per day. Follow up consultations will monitor individual progress, tolerability and adverse events. Usual care, if deemed appropriate by the study doctor, may include a referral for physical or manual therapy and/or prescription of analgesic medication. Participants, doctors and researchers collecting participant data will be blinded to treatment allocation. Participants will be assessed at baseline and at weeks 2, 4, 8, 12, 26 and 52. The primary outcome will determine the efficacy of pregabalin in reducing leg pain intensity. Secondary outcomes will include back pain intensity, disability and quality of life. Data analysis will be blinded and by intention-to-treat. A parallel economic evaluation will be conducted from health sector and societal perspectives. DISCUSSION: This study will establish the efficacy of pregabalin in reducing leg pain intensity in patients with sciatica and provide important information regarding the effect of pregabalin treatment on disability and quality of life. The impact of this research may allow the future development of a cost-effective conservative treatment strategy for patients with sciatica. TRIAL REGISTRATION: ClinicalTrial.gov, ACTRN 12613000530729 BioMed Central 2013-07-11 /pmc/articles/PMC3711833/ /pubmed/23845078 http://dx.doi.org/10.1186/1745-6215-14-213 Text en Copyright © 2013 Mathieson et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Mathieson, Stephanie
Maher, Christopher G
McLachlan, Andrew J
Latimer, Jane
Koes, Bart W
Hancock, Mark J
Harris, Ian
Day, Richard O
Pik, Justin
Jan, Stephen
Billot, Laurent
Lin, Chung-Wei Christine
PRECISE - pregabalin in addition to usual care for sciatica: study protocol for a randomised controlled trial
title PRECISE - pregabalin in addition to usual care for sciatica: study protocol for a randomised controlled trial
title_full PRECISE - pregabalin in addition to usual care for sciatica: study protocol for a randomised controlled trial
title_fullStr PRECISE - pregabalin in addition to usual care for sciatica: study protocol for a randomised controlled trial
title_full_unstemmed PRECISE - pregabalin in addition to usual care for sciatica: study protocol for a randomised controlled trial
title_short PRECISE - pregabalin in addition to usual care for sciatica: study protocol for a randomised controlled trial
title_sort precise - pregabalin in addition to usual care for sciatica: study protocol for a randomised controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3711833/
https://www.ncbi.nlm.nih.gov/pubmed/23845078
http://dx.doi.org/10.1186/1745-6215-14-213
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