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Valsartan Amlodipine Randomized Trial (VART): Design, Methods, and Preliminary Results.

Valsartan Amlodipine Randomized Trial (VART): Design, Methods, and Preliminary Results. Research Abstract Details 

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  • Valsartan Amlodipine Randomized Trial (VART): Design, Methods, and Preliminary Results. Abstract Text:

    keiko nakayamaKeiko Nakayama,yoichi kuwabaraYoichi Kuwabara,masao daimonMasao Daimon,satoshi shindoSatoshi Shindo,miwa fujitaMiwa Fujita,hiroya narumiHiroya Narumi,hiroshi mizumaHiroshi Mizuma,issei komuroIssei Komuro,keiko nakayamaKeiko Nakayama,yoichi kuwabaraYoichi Kuwabara,masao daimonMasao Daimon,satoshi shindoSatoshi Shindo,miwa fujitaMiwa Fujita,hiroya narumiHiroya Narumi,hiroshi mizumaHiroshi Mizuma,issei komuroIssei Komuro,

    Antihypertensive therapy has been well established to reduce hypertension-related morbidity and mortality, but the optimal therapy for Japanese patients remains unknown. The Valsartan Amlodipine Randomized Trial (VART), a prospective randomized open-label trial, was designed to determine whether treatment with an angiotensin II type 1 receptor blocker (valsartan) or a calcium channel blocker (amlodipine) lowers cardiovascular disease events in essential hypertensives in Japan. Registration, randomization and data entry were performed over the Internet. The minimization method (to control for age, gender, blood pressure level and history) was used at random assignment to ensure that the background factors were equivalent between the groups at baseline. After the registration, patients were followed-up for cardiovascular events (primary endpoints), echocardiography, (123)I-metaiodobenzylguanidine (MIBG) imaging, laboratory tests and blood pressure for 3 years. Currently, 797 patients have been enrolled and assigned to two groups: a valsartan (n=399) and an amlodipine (n=398) group. At baseline, controlled factors (age, gender, blood pressure level, and left ventricular hypertrophy) and the proportions of patients with diabetes and hyperlipidemia were equally allocated. At 12 months, both drugs evenly and significantly lowered blood pressure to the target level (valsartan: 133/79 mmHg; amlodipine: 132/79 mmHg). In conclusion, by combining the data on cardiovascular events with the results of echocardiographic, radionuclide imaging, and blood/urine studies, the VART study will provide mechanistic insights into the clinical outcomes and treatment effects of the trial. (Hypertens Res 2008; 31: 21-28).

    Valsartan Amlodipine Randomized Trial (VART): Design, Methods, and Preliminary Results. Publishing Authors By Initials

    k nakayamaK Nakayama,y kuwabaraY Kuwabara,m daimonM Daimon,s shindoS Shindo,m fujitaM Fujita,h narumiH Narumi,h mizumaH Mizuma,i komuroI Komuro,k nakayamaK Nakayama,y kuwabaraY Kuwabara,m daimonM Daimon,s shindoS Shindo,m fujitaM Fujita,h narumiH Narumi,h mizumaH Mizuma,i komuroI Komuro,

    For similar abstracts research abstracts see: abstracts research

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    Valsartan Amlodipine Randomized Trial (VART): Design, Methods, and Preliminary Results. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Hypertension research : official journal of the Ja

    VOLUME: 31

    Page Numbers: 21-8

    Journal Abbreviation: Hypertens. Res.

    ISSN: 0916-9636

    DAY: 24

    MONTH: Jan

    YEAR: 2008

    Valsartan Amlodipine Randomized Trial (VART): Design, Methods, and Preliminary Results. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 9307690

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    Grant and Affiliation Information for Valsartan Amlodipine Randomized Trial (VART): Design, Methods, and Preliminary Results.

    AFFILIATION: Department of Cardiovascular Science and Medicine, Chiba University Graduate School of Medicine.

    Country: Japan

    Japan Research PublicationJapan Research Publication

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    MEDLINETA: Hypertens Res

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