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Chronic non-cancer pain: Focus on once-daily tramadol formulations

Despite progress in pain management, chronic non-cancer pain (CNCP) represents still a clinical challenge. The efficacy and safety profile of tramadol make it suitable as a long-term treatment in a variety of CNCP conditions. New once-daily (OD) formulations of tramadol have been marketed in various...

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Detalles Bibliográficos
Autores principales: Coluzzi, Flaminia, Mattia, Consalvo
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376086/
https://www.ncbi.nlm.nih.gov/pubmed/18473006
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author Coluzzi, Flaminia
Mattia, Consalvo
author_facet Coluzzi, Flaminia
Mattia, Consalvo
author_sort Coluzzi, Flaminia
collection PubMed
description Despite progress in pain management, chronic non-cancer pain (CNCP) represents still a clinical challenge. The efficacy and safety profile of tramadol make it suitable as a long-term treatment in a variety of CNCP conditions. New once-daily (OD) formulations of tramadol have been marketed in various countries, in order to offer the advantage of a reduced dosing regimen and to improve patients’ compliance. This review focuses on the technology, pharmacology, clinical efficacy, and safety of different once-daily tramadol formulations. Hydrophilic vs hydrophobic matrix systems and newer technologies used in once-daily formulations to control drug delivery are discussed. Three randomized controlled trials (RCTs) established OD tramadol analgesic efficacy to be superior to that of placebo for pain management and functional improvement in patients with osteoarthritis. Three RCTs demonstrated similar rates of efficacy between OD tramadol and immediate-release (IR) or sustained-release (SR) formulations, with a better adverse events profile. An open trial on long term tolerability showed that OD tramadol is generally safe in rheumatological pain treatment.
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spelling pubmed-23760862008-05-12 Chronic non-cancer pain: Focus on once-daily tramadol formulations Coluzzi, Flaminia Mattia, Consalvo Ther Clin Risk Manag Review Despite progress in pain management, chronic non-cancer pain (CNCP) represents still a clinical challenge. The efficacy and safety profile of tramadol make it suitable as a long-term treatment in a variety of CNCP conditions. New once-daily (OD) formulations of tramadol have been marketed in various countries, in order to offer the advantage of a reduced dosing regimen and to improve patients’ compliance. This review focuses on the technology, pharmacology, clinical efficacy, and safety of different once-daily tramadol formulations. Hydrophilic vs hydrophobic matrix systems and newer technologies used in once-daily formulations to control drug delivery are discussed. Three randomized controlled trials (RCTs) established OD tramadol analgesic efficacy to be superior to that of placebo for pain management and functional improvement in patients with osteoarthritis. Three RCTs demonstrated similar rates of efficacy between OD tramadol and immediate-release (IR) or sustained-release (SR) formulations, with a better adverse events profile. An open trial on long term tolerability showed that OD tramadol is generally safe in rheumatological pain treatment. Dove Medical Press 2007-10 2007-10 /pmc/articles/PMC2376086/ /pubmed/18473006 Text en © 2007 Dove Medical Press Limited. All rights reserved
spellingShingle Review
Coluzzi, Flaminia
Mattia, Consalvo
Chronic non-cancer pain: Focus on once-daily tramadol formulations
title Chronic non-cancer pain: Focus on once-daily tramadol formulations
title_full Chronic non-cancer pain: Focus on once-daily tramadol formulations
title_fullStr Chronic non-cancer pain: Focus on once-daily tramadol formulations
title_full_unstemmed Chronic non-cancer pain: Focus on once-daily tramadol formulations
title_short Chronic non-cancer pain: Focus on once-daily tramadol formulations
title_sort chronic non-cancer pain: focus on once-daily tramadol formulations
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376086/
https://www.ncbi.nlm.nih.gov/pubmed/18473006
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