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dc.contributor.author박시훈-
dc.date.accessioned2016-08-28T11:08:43Z-
dc.date.available2016-08-28T11:08:43Z-
dc.date.issued2012-
dc.identifier.issn1175-3277-
dc.identifier.otherOAK-13771-
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/229723-
dc.description.abstractBackground: Despite recommendations for more intensive treatment and the availability of several effective treatments, hypertension remains uncontrolled in many patients. Objective: The aim of this study was to determine the dose-response relationship and assess the efficacy and safety of amlodipine or losartan monotherapy and amlodipine camsylate/losartan combination therapy in patients with essential hypertension. Methods: This was an 8-week, randomized, double-blind, factorial design, phase II, multicenter study conducted in outpatient hospital clinics among adult patients aged 18-75 years with essential hypertension. At screening, patients received placebo for 2-4 weeks. Eligible patients (n = 320) were randomized to one of eight treatment groups: amlodipine 5mg or 10 mg, losartan 50mg or 100 mg, amlodipine camsylate/losartan 5mg/50 mg, 5mg/100 mg, 10 mg/50 mg, or 10 mg/100 mg. Main Outcome Measures: The assumption of strict superiority was estimated using the mean change in sitting diastolic blood pressure (DBP) at 8 weeks. Safety was monitored through physical examinations, vital signs, laboratory test results, ECG, and adverse events. Results: The reduction in DBP at 8 weeks was significantly greater in patients treated with the combination therapies compared with the respective monotherapies for all specified comparisons except amlodipine camsylate/losartan 10 mg/100mg versus amlodipine 10 mg. The incidence of adverse events in the group of patients treated with the amlodipine camsylate/losartan 10 mg/50 mg combination tended to be higher than for any other group (27.9%, 12/43); however, the effect was not statistically significant. Conclusion: Combination amlodipine camsylate/losartan (5 mg/50 mg, 5mg/100mg and 10 mg/50 mg) resulted in significantly greater BP lowering compared with amlodipine or losartan monotherapy, and was determined to be generally safe and tolerable in patients with essential hypertension. © 2012 Adis Data Information BV. All rights reserved.-
dc.languageEnglish-
dc.titleEvaluation of the dose-response relationship of amlodipine and losartan combination in patients with essential hypertension: An 8-week, randomized, double-blind, factorial, phase II, multicenter study-
dc.typeArticle-
dc.relation.issue1-
dc.relation.volume12-
dc.relation.indexSCIE-
dc.relation.indexSCOPUS-
dc.relation.startpage35-
dc.relation.lastpage47-
dc.relation.journaltitleAmerican Journal of Cardiovascular Drugs-
dc.identifier.doi10.2165/11597170-000000000-00000-
dc.identifier.wosidWOS:000301278100004-
dc.identifier.scopusid2-s2.0-84863023379-
dc.author.googlePark C.-G.-
dc.author.googleYoun H.-J.-
dc.author.googleChae S.-C.-
dc.author.googleYang J.-Y.-
dc.author.googleKim M.-H.-
dc.author.googleHong T.-J.-
dc.author.googleKim C.H.-
dc.author.googleKim J.J.-
dc.author.googleHong B.-K.-
dc.author.googleJeong J.-W.-
dc.author.googlePark S.-H.-
dc.author.googleKwan J.-
dc.author.googleChoi Y.-J.-
dc.author.googleCho S.-Y.-
dc.contributor.scopusid박시훈(9737584900;57191750840)-
dc.date.modifydate20221123115020-
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의과대학 > 의학과 > Journal papers
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