Critical appraisal of ramelteon in the treatment of insomnia

Ramelteon is the first member of a novel class of hypnotics and acts as a selective melatonin receptor agonist. In 2005, ramelteon was approved by the US Food and Drug Administration for the treatment of insomnia characterized by sleep onset problems. Its unique mechanism of action made it a promisi...

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Main Authors: Mets, Monique AJ, van Deventer, Kenny R, Olivier, Berend, Verster, Joris C
Format: Online
Language:English
Published: Dove Medical Press 2010
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630951/
id pubmed-3630951
recordtype oai_dc
spelling pubmed-36309512013-04-24 Critical appraisal of ramelteon in the treatment of insomnia Mets, Monique AJ van Deventer, Kenny R Olivier, Berend Verster, Joris C Review Ramelteon is the first member of a novel class of hypnotics and acts as a selective melatonin receptor agonist. In 2005, ramelteon was approved by the US Food and Drug Administration for the treatment of insomnia characterized by sleep onset problems. Its unique mechanism of action made it a promising candidate compared with the widely used hypnotics that act on the benzodiazepine receptor complex. Several studies have examined its efficacy and safety as a hypnotic agent. The primary efficacy of ramelteon was found to lie in a decrease in latency to persistent sleep, as measured by polysomnographic tests. Other sleep-related measures, such as total sleep time and number of nightly awakenings, show less pronounced improvement when treated with ramelteon. In addition, no rebound insomnia or abuse potential was observed in clinical studies. Although additional studies are necessary, current data on the acute and next-morning effects of ramelteon did not indicate cognitive or psychomotor impairment. Overall, ramelteon is safe and well tolerated, although some questions remain regarding its long-term efficacy and safety. These issues and possibilities for use in other patient groups should be addressed in future research. Dove Medical Press 2010-11-10 /pmc/articles/PMC3630951/ /pubmed/23616713 http://dx.doi.org/10.2147/NSS.S6846 Text en © 2010 Mets et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Mets, Monique AJ
van Deventer, Kenny R
Olivier, Berend
Verster, Joris C
spellingShingle Mets, Monique AJ
van Deventer, Kenny R
Olivier, Berend
Verster, Joris C
Critical appraisal of ramelteon in the treatment of insomnia
author_facet Mets, Monique AJ
van Deventer, Kenny R
Olivier, Berend
Verster, Joris C
author_sort Mets, Monique AJ
title Critical appraisal of ramelteon in the treatment of insomnia
title_short Critical appraisal of ramelteon in the treatment of insomnia
title_full Critical appraisal of ramelteon in the treatment of insomnia
title_fullStr Critical appraisal of ramelteon in the treatment of insomnia
title_full_unstemmed Critical appraisal of ramelteon in the treatment of insomnia
title_sort critical appraisal of ramelteon in the treatment of insomnia
description Ramelteon is the first member of a novel class of hypnotics and acts as a selective melatonin receptor agonist. In 2005, ramelteon was approved by the US Food and Drug Administration for the treatment of insomnia characterized by sleep onset problems. Its unique mechanism of action made it a promising candidate compared with the widely used hypnotics that act on the benzodiazepine receptor complex. Several studies have examined its efficacy and safety as a hypnotic agent. The primary efficacy of ramelteon was found to lie in a decrease in latency to persistent sleep, as measured by polysomnographic tests. Other sleep-related measures, such as total sleep time and number of nightly awakenings, show less pronounced improvement when treated with ramelteon. In addition, no rebound insomnia or abuse potential was observed in clinical studies. Although additional studies are necessary, current data on the acute and next-morning effects of ramelteon did not indicate cognitive or psychomotor impairment. Overall, ramelteon is safe and well tolerated, although some questions remain regarding its long-term efficacy and safety. These issues and possibilities for use in other patient groups should be addressed in future research.
publisher Dove Medical Press
publishDate 2010
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3630951/
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