Eszopiclone versus zopiclone in the treatment of insomnia

Detalhes bibliográficos
Autor(a) principal: Pinto Júnior, Luciano Ribeiro [UNIFESP]
Data de Publicação: 2016
Outros Autores: Bittencourt, Lia Rita Azeredo [UNIFESP], Treptow, Erika Cristine [UNIFESP], Braga, Luciano Rotella [UNIFESP], Tufik, Sergio [UNIFESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://repositorio.unifesp.br/handle/11600/49606
http://dx.doi.org/10.6061/clinics/2016(01)02
Resumo: OBJECTIVE: To determine the therapeutic effects of two selective GABA-A agonists, zopiclone and eszopiclone, in the treatment of insomnia. METHODS: This study comprised a phase III, single-center, randomized, double-blind, double-dummy, parallel-group, non-inferiority trial. Patients were randomized to receive zopiclone 7.5 mg or eszopiclone 3 mg, both orally, for four weeks. In total, 199 patients were evaluated during two visits and then followed for at least six weeks. The primary endpoint was the Insomnia Severity Index after four weeks of treatment. Secondary endpoints were obtained through polysomnography data, including total sleep time, sleep latency and sleep efficiency. The frequency of adverse events was also analyzed. ClinicalTrials.gov: NCT01100164. RESULTS: The primary efficacy analysis demonstrated the non-inferiority of eszopiclone over zopiclone. Analysis of objective parameters assessed by polysomnography showed that eszopiclone increased total sleep time and also improved sleep efficiency. The safety profile of both study treatments was similar and the most common events reported in both groups were dysgeusia, headache, dizziness, irritability and nausea. Adverse events were observed in 223 patients, 109 (85.2%) in the eszopiclone group and 114 (87.7%) in the zopiclone group. CONCLUSION: Based on the Insomnia Severity Index at the end of four weeks of treatment, eszopiclone demonstrated efficacy comparable to that of zopiclone in the treatment of insomnia, increasing total sleep time as well as sleep efficiency according to polysomnography.
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spelling Pinto Júnior, Luciano Ribeiro [UNIFESP]Bittencourt, Lia Rita Azeredo [UNIFESP]Treptow, Erika Cristine [UNIFESP]Braga, Luciano Rotella [UNIFESP]Tufik, Sergio [UNIFESP]2019-01-21T10:30:08Z2019-01-21T10:30:08Z2016Clinics. Sao paulo, v. 71, n. 1, p. 5-9, 2016.1807-5932http://repositorio.unifesp.br/handle/11600/49606http://dx.doi.org/10.6061/clinics/2016(01)02S1807-59322016000100005.pdfS1807-5932201600010000510.6061/clinics/2016(01)02WOS:000370621800002OBJECTIVE: To determine the therapeutic effects of two selective GABA-A agonists, zopiclone and eszopiclone, in the treatment of insomnia. METHODS: This study comprised a phase III, single-center, randomized, double-blind, double-dummy, parallel-group, non-inferiority trial. Patients were randomized to receive zopiclone 7.5 mg or eszopiclone 3 mg, both orally, for four weeks. In total, 199 patients were evaluated during two visits and then followed for at least six weeks. The primary endpoint was the Insomnia Severity Index after four weeks of treatment. Secondary endpoints were obtained through polysomnography data, including total sleep time, sleep latency and sleep efficiency. The frequency of adverse events was also analyzed. ClinicalTrials.gov: NCT01100164. RESULTS: The primary efficacy analysis demonstrated the non-inferiority of eszopiclone over zopiclone. Analysis of objective parameters assessed by polysomnography showed that eszopiclone increased total sleep time and also improved sleep efficiency. The safety profile of both study treatments was similar and the most common events reported in both groups were dysgeusia, headache, dizziness, irritability and nausea. Adverse events were observed in 223 patients, 109 (85.2%) in the eszopiclone group and 114 (87.7%) in the zopiclone group. CONCLUSION: Based on the Insomnia Severity Index at the end of four weeks of treatment, eszopiclone demonstrated efficacy comparable to that of zopiclone in the treatment of insomnia, increasing total sleep time as well as sleep efficiency according to polysomnography.Associacao Fundo de Incentivo a Pesquisa (AFIP)Universidade Federal de São Paulo (UNIFESP), Departamento de Psicobiologia, São Paulo/, SP, BrazilUniversidade Federal de São Paulo (UNIFESP), Departamento de Psicobiologia, São Paulo/, SP, BrazilWeb of Science5-9engHospital clinicas, univ sao pauloClinicsInsomniaZopicloneEszopiclonePolysomnographySleep DisturbancesNightly TreatmentHypnoticsPrevalenceEfficacyAdultsIndexEszopiclone versus zopiclone in the treatment of insomniainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP11600/496062021-10-05 21:33:38.217metadata only accessoai:repositorio.unifesp.br:11600/49606Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestopendoar:34652021-10-06T00:33:38Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.en.fl_str_mv Eszopiclone versus zopiclone in the treatment of insomnia
title Eszopiclone versus zopiclone in the treatment of insomnia
spellingShingle Eszopiclone versus zopiclone in the treatment of insomnia
Pinto Júnior, Luciano Ribeiro [UNIFESP]
Insomnia
Zopiclone
Eszopiclone
PolysomnographySleep Disturbances
Nightly Treatment
Hypnotics
Prevalence
Efficacy
Adults
Index
title_short Eszopiclone versus zopiclone in the treatment of insomnia
title_full Eszopiclone versus zopiclone in the treatment of insomnia
title_fullStr Eszopiclone versus zopiclone in the treatment of insomnia
title_full_unstemmed Eszopiclone versus zopiclone in the treatment of insomnia
title_sort Eszopiclone versus zopiclone in the treatment of insomnia
author Pinto Júnior, Luciano Ribeiro [UNIFESP]
author_facet Pinto Júnior, Luciano Ribeiro [UNIFESP]
Bittencourt, Lia Rita Azeredo [UNIFESP]
Treptow, Erika Cristine [UNIFESP]
Braga, Luciano Rotella [UNIFESP]
Tufik, Sergio [UNIFESP]
author_role author
author2 Bittencourt, Lia Rita Azeredo [UNIFESP]
Treptow, Erika Cristine [UNIFESP]
Braga, Luciano Rotella [UNIFESP]
Tufik, Sergio [UNIFESP]
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Pinto Júnior, Luciano Ribeiro [UNIFESP]
Bittencourt, Lia Rita Azeredo [UNIFESP]
Treptow, Erika Cristine [UNIFESP]
Braga, Luciano Rotella [UNIFESP]
Tufik, Sergio [UNIFESP]
dc.subject.eng.fl_str_mv Insomnia
Zopiclone
Eszopiclone
PolysomnographySleep Disturbances
Nightly Treatment
Hypnotics
Prevalence
Efficacy
Adults
Index
topic Insomnia
Zopiclone
Eszopiclone
PolysomnographySleep Disturbances
Nightly Treatment
Hypnotics
Prevalence
Efficacy
Adults
Index
description OBJECTIVE: To determine the therapeutic effects of two selective GABA-A agonists, zopiclone and eszopiclone, in the treatment of insomnia. METHODS: This study comprised a phase III, single-center, randomized, double-blind, double-dummy, parallel-group, non-inferiority trial. Patients were randomized to receive zopiclone 7.5 mg or eszopiclone 3 mg, both orally, for four weeks. In total, 199 patients were evaluated during two visits and then followed for at least six weeks. The primary endpoint was the Insomnia Severity Index after four weeks of treatment. Secondary endpoints were obtained through polysomnography data, including total sleep time, sleep latency and sleep efficiency. The frequency of adverse events was also analyzed. ClinicalTrials.gov: NCT01100164. RESULTS: The primary efficacy analysis demonstrated the non-inferiority of eszopiclone over zopiclone. Analysis of objective parameters assessed by polysomnography showed that eszopiclone increased total sleep time and also improved sleep efficiency. The safety profile of both study treatments was similar and the most common events reported in both groups were dysgeusia, headache, dizziness, irritability and nausea. Adverse events were observed in 223 patients, 109 (85.2%) in the eszopiclone group and 114 (87.7%) in the zopiclone group. CONCLUSION: Based on the Insomnia Severity Index at the end of four weeks of treatment, eszopiclone demonstrated efficacy comparable to that of zopiclone in the treatment of insomnia, increasing total sleep time as well as sleep efficiency according to polysomnography.
publishDate 2016
dc.date.issued.fl_str_mv 2016
dc.date.accessioned.fl_str_mv 2019-01-21T10:30:08Z
dc.date.available.fl_str_mv 2019-01-21T10:30:08Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.citation.fl_str_mv Clinics. Sao paulo, v. 71, n. 1, p. 5-9, 2016.
dc.identifier.uri.fl_str_mv http://repositorio.unifesp.br/handle/11600/49606
http://dx.doi.org/10.6061/clinics/2016(01)02
dc.identifier.issn.none.fl_str_mv 1807-5932
dc.identifier.file.none.fl_str_mv S1807-59322016000100005.pdf
dc.identifier.scielo.none.fl_str_mv S1807-59322016000100005
dc.identifier.doi.none.fl_str_mv 10.6061/clinics/2016(01)02
dc.identifier.wos.none.fl_str_mv WOS:000370621800002
identifier_str_mv Clinics. Sao paulo, v. 71, n. 1, p. 5-9, 2016.
1807-5932
S1807-59322016000100005.pdf
S1807-59322016000100005
10.6061/clinics/2016(01)02
WOS:000370621800002
url http://repositorio.unifesp.br/handle/11600/49606
http://dx.doi.org/10.6061/clinics/2016(01)02
dc.language.iso.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Clinics
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 5-9
dc.publisher.none.fl_str_mv Hospital clinicas, univ sao paulo
publisher.none.fl_str_mv Hospital clinicas, univ sao paulo
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv
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