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Efficacy and safety of combination therapy with vildagliptin and metformin versus metformin up-titration in Chinese patients with type 2 diabetes mellitus: study design and rationale of the vision study

机译:维达列汀和二甲双胍联合治疗与二甲双胍调高联合治疗在中国2型糖尿病患者中的疗效和安全性:研究设计和视觉研究的原理

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Background and aim Limitations of the currently recommended stepwise treatment pathway for type 2 diabetes mellitus (T2DM), especially the failure of monotherapies to maintain good glycemic control, have prompted use of early, more aggressive combination therapies. The VISION study is designed to explore the efficacy and safety of vildagliptin as an add-on to metformin therapy compared with up-titration of metformin monotherapy in Chinese patients with T2DM. Methods VISION, a 24-week, phase 4, prospective, randomized, multicenter, open-label, parallel-group study, will include 3312 Chinese T2DM patients aged ≥18 years who are inadequately controlled (6.5% >HbA1c ≤9%) by metformin (750–1000 mg/day). Eligible patients will be randomized to receive either vildagliptin plus metformin or up-titration of metformin monotherapy (5:1). Patients will also be subgrouped (1:1:1:1) based on their age and body mass index (BMI): 2; 2; ≥60 years and 2; and ≥60 years and ≥24 kg/m2. Conclusion The VISION study will test the hypothesis that early use of combination therapy with vildagliptin and metformin will provide good glycemic control and will be better tolerated than up-titration of metformin monotherapy. The study will also correlate these benefits with age and BMI.
机译:背景和目的目前推荐的2型糖尿病(T2DM)逐步治疗途径的局限性,尤其是单一疗法未能维持良好的血糖控制的局限性促使人们采用早期,更具攻击性的联合疗法。 VISION研究旨在探讨维达列汀作为二甲双胍治疗的补充剂与中国2型糖尿病患者二甲双胍单药调高剂量相比的疗效和安全性。方法VISION是一项为期24周的第4期,前瞻性,随机,多中心,开放标签,平行分组的研究,将纳入3312例年龄≥18岁的中国T2DM患者,他们的控制不足(6.5%> HbA1c≤9%)二甲双胍(750-1000毫克/天)。符合条件的患者将被随机分配接受维格列汀加二甲双胍或二甲双胍单药调高剂量(5:1)。根据年龄和体重指数(BMI):2 将患者分为亚组(1:1:1:1); 2 ; ≥60岁2 ; ≥60岁且≥24kg / m 2 。结论VISION研究将验证以下假设,即与维达列汀和二甲双胍联合使用的早期治疗将提供良好的血糖控制,并且比二甲双胍单药的调高耐受性更好。该研究还将这些益处与年龄和BMI相关联。

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