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dc.contributor.authorRullán García, Manuel
dc.contributor.authorBulilete, Oana
dc.contributor.authorLeiva Rus, Alfonso
dc.contributor.authorSoler Mieras, Aina
dc.contributor.authorRoca, Antonia
dc.contributor.authorJose Gonzalez-Bals, Maria
dc.contributor.authorLorente, Patricia
dc.contributor.authorLlobera Cànaves, Joan
dc.contributor.authorPHN Grp
dc.date.accessioned2024-07-11T09:07:32Z
dc.date.available2024-07-11T09:07:32Z
dc.date.issued2017-01-14
dc.identifier.citationRullan M, Bulilete O, Leiva A, Soler Mieras A, Roca Jaume A, Gonzalez-Bals MJ, et al. Efficacy of gabapentin for prevention of postherpetic neuralgia: study protocol for a randomized controlled clinical trial. Trials. 2017 Jan 14;18:24.en
dc.identifier.issn1745-6215
dc.identifier.otherhttp://hdl.handle.net/20.500.13003/9987
dc.identifier.urihttp://hdl.handle.net/20.500.12105/20403
dc.description.abstractBackground: Postherpetic neuralgia (PHN) is a chronic neuropathic pain that results from alterations of the peripheral nervous system in areas affected by the herpes zoster virus. The symptoms include pain, paresthesia, dysesthesia, hyperalgesia, and allodynia. Despite the availability of pharmacological treatments to control these symptoms, no treatments are available to control the underlying pathophysiology responsible for this disabling condition. Methods/design: Patients with herpes zoster who are at least 50 years old and have a pain score of 4 or higher on a visual analogue scale (VAS) will be recruited. The aim is to recruit 134 patients from the practices of general physicians. Participants will be randomized to receive gabapentin to a maximum of 1800 mg/day for 5 weeks or placebo. Both arms will receive 1000-mg caplets of valacyclovir three times daily for 7 days (initiated within 72 h of the onset of symptoms) and analgesics as needed. The primary outcome measure is the percentage of patients with a VAS pain score of 0 at 12 weeks from rash onset. The secondary outcomes measures are changes in quality of life (measured by the SF-12 questionnaire), sleep disturbance (measured by the Medical Outcomes Study Sleep Scale), and percentage of patients with neuropathic pain (measured by the Douleur Neuropathique in 4 Questions). Discussion: Gabapentin is an anticonvulsant type of analgesic that could prevent the onset of PHN by its antihypersensitivity action in dorsal horn neurons.en
dc.description.sponsorshipThis study was funded by the Ministry of Health, Carlos III Institute (grant PI12/01813). We also received support from the Health Promotion and Preventive Activities-Primary Health Care Network, sustained by the Ministry of Health, Carlos III Institute, Redes Tematicas de Investigacion Cooperativa en Salud (RETIC) award RD12/0005/0011, co-financed by the European Union European Regional Development Fund. The funders had no role in the study design, data collection, analysis, decision to publish, or preparation of the manuscript.es_ES
dc.language.isoengen
dc.publisherBioMed Central (BMC) en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectPostherpetic neuralgia
dc.subjectGabapentin
dc.subjectHerpes zoster
dc.subjectPrevention
dc.subjectPrimary health care
dc.subject.meshAnalgesics *
dc.subject.meshAmines *
dc.subject.meshCyclohexanecarboxylic Acids *
dc.subject.meshClinical Protocols *
dc.subject.meshSpain *
dc.subject.meshAntiviral Agents *
dc.subject.meshHumans *
dc.subject.meshAcyclovir *
dc.subject.meshMiddle Aged *
dc.subject.meshDouble-Blind Method *
dc.subject.meshgamma-Aminobutyric Acid *
dc.subject.meshPain Measurement *
dc.subject.meshHerpes Zoster *
dc.subject.meshResearch Design *
dc.subject.meshMale *
dc.subject.meshQuality of Life *
dc.subject.meshTime Factors *
dc.subject.meshFemale *
dc.subject.meshSleep *
dc.subject.meshTreatment Outcome *
dc.subject.meshNeuralgia, Postherpetic *
dc.subject.meshValine *
dc.subject.meshSurveys and Questionnaires *
dc.titleEfficacy of gabapentin for prevention of postherpetic neuralgia: study protocol for a randomized controlled clinical trialen
dc.typeresearch articleen
dc.rights.licenseAttribution 4.0 International*
dc.identifier.pubmedID28088231es_ES
dc.format.volume18es_ES
dc.format.page24es_ES
dc.identifier.doi10.1186/s13063-016-1729-y
dc.relation.publisherversionhttps://dx.doi.org/10.1186/s13063-016-1729-yen
dc.identifier.journalTrialses_ES
dc.rights.accessRightsopen accessen
dc.subject.decsSueño*
dc.subject.decsResultado del Tratamiento*
dc.subject.decsValina*
dc.subject.decsFactores de Tiempo*
dc.subject.decsFemenino*
dc.subject.decsHerpes Zóster*
dc.subject.decsÁcido gamma-Aminobutírico*
dc.subject.decsMasculino*
dc.subject.decsMétodo Doble Ciego*
dc.subject.decsHumanos*
dc.subject.decsPersona de Mediana Edad*
dc.subject.decsCalidad de Vida*
dc.subject.decsProyectos de Investigación*
dc.subject.decsAciclovir*
dc.subject.decsProtocolos Clínicos*
dc.subject.decsDimensión del Dolor*
dc.subject.decsAminas*
dc.subject.decsEncuestas y Cuestionarios*
dc.subject.decsAnalgésicos*
dc.subject.decsAntivirales*
dc.subject.decsÁcidos Ciclohexanocarboxílicos*
dc.subject.decsEspaña*
dc.subject.decsNeuralgia Posherpética*
dc.identifier.scopus2-s2.0-85009387021
dc.identifier.wos392029500002
dc.identifier.puiL614054550


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Attribution 4.0 International
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