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Comparison of once-daily versus twice-daily combination of Ropinirole prolonged release in Parkinson¿s disease

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dc.contributor.authorYun, Ji Young-
dc.contributor.authorKim, Han-Joon-
dc.contributor.authorLee, Jee-Young-
dc.contributor.authorKim, Young Eun-
dc.contributor.authorKim, Ji Seon-
dc.contributor.authorKim, Jong-Min-
dc.contributor.authorJeon, Beom S-
dc.date.accessioned2013-10-02T04:35:09Z-
dc.date.available2013-10-02T04:35:09Z-
dc.date.issued2013-09-02-
dc.identifier.citationBMC Neurology Vol.13 No.113, pp.1-7ko_KR
dc.identifier.issn1471-2377-
dc.identifier.urihttps://hdl.handle.net/10371/83494-
dc.identifier.urihttp://www.biomedcentral.com/1471-2377/13/113-
dc.descriptionTrial registration : This study is registered with ClinicalTrials.gov, number NCT00986245.ko_KR
dc.description.abstractBackground : Ropinirole prolonged release (RPR) is a once-daily formulation. However, there may be individual pharmacokinetic differences so that multiple dosing may be preferred in some individuals. This study compares once-daily and twice-daily RPR in patients with Parkinsons disease.
Methods : This study was an open-label crossover study. We enrolled Parkinsons disease patients on dopamine agonist therapy with unsatisfactory control such as motor fluctuation, dyskinesia and sleep-related problems. Agonists were switched into equivalent dose of RPR. Subjects were consecutively enrolled into either once-daily first or twice-daily first groups, and received the same amount of RPR in a single and two divided dosing for 8weeks respectively in a crossover manner without a washout period.
The primary outcome was a questionnaire of the preference completed by patients in the last visit. The secondary outcome measures included the Unified Parkinsons Disease Rating Scale part 3 (mUPDRS), Hoehn and Yahr stage (H&Y); sleep questionnaire including overall quality of sleep, nocturnal off symptoms and early morning symptoms; Epworth Sleep Scale (ESS); compliances and patient global impression (PGI).
Results : A total of 82 patients were enrolled and 61 completed the study. 31 patients preferred twice-daily regimen, 17 preferred the once-daily regimen, and 13 had no preference. Their mean mUPDRS, H&Y, ESS, sleep quality, compliance and adverse events were not statistically different in both regimens. PGI-improvement on wearing off defined was better in twice-daily dosing regimen. Conclusions : RPR is a once-daily formulation, but multiple dosing was preferred in many patients. Multiple dosing of RPR might be a therapeutic option if once-daily dosing is unsatisfactory.
ko_KR
dc.description.sponsorshipThis study was supported by a grant of the Korea Health technology R&D Project, Ministry of Health & Welfare, Republic of Korea. (A101273, BSJ).ko_KR
dc.language.isoenko_KR
dc.publisherBioMed Central Ltd.ko_KR
dc.subjectParkinson’s diseaseko_KR
dc.subjectMotor controlko_KR
dc.subjectMovement disordersko_KR
dc.subjectDopamine agonistko_KR
dc.titleComparison of once-daily versus twice-daily combination of Ropinirole prolonged release in Parkinson¿s diseaseko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor윤지영-
dc.contributor.AlternativeAuthor김한준-
dc.contributor.AlternativeAuthor이재영-
dc.contributor.AlternativeAuthor김영은-
dc.contributor.AlternativeAuthor김지선-
dc.contributor.AlternativeAuthor김종민-
dc.identifier.doi10.1186/1471-2377-13-113-
dc.citation.journaltitleBMC Neurology-
dc.language.rfc3066en-
dc.description.versionPeer Reviewed-
dc.rights.holderJi Yun et al.; licensee BioMed Central Ltd.-
dc.date.updated2013-10-01T19:30:57Z-
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