JPRN-UMIN000004970已完成未知
Randomised, parallel-group trial to compare the efficacy and safety of GLP-1 analogue: liraglutide and DPP-4 inhibitor: sitagliptin as combination therapy in subjects with type 2 diabetes using sulfonylurea. - Randomised, parallel-group trial to compare the efficacy and safety of GLP-1 analogue: liraglutide and DPP-4 inhibitor: sitagliptin as combination therapy in subjects with type 2 diabetes using sulfonylurea.
Japan Diabetes Clinical Data Management Study Group0 个研究点目标入组 152 人开始时间: 2011年2月1日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 152
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18years-old 至 80years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1. Known hypoglycemia unawareness or recurrent major hypoglycemia. 2. Patients with proliferative retinopathy or maculopathy requiring acute treatment 3. Impaired hepatic function [GOT(AST)>80IU/L or GPT(ALT)>80IU/L], Impaired renal function (serum-creatinine; >=1.7mg/dL) 4. Patients with allergic reaction to the trial products or related products 5. Patients with known or previous malignant tumour and are strongly suspected of recurrence 6. Pregnant, breast-feeding (within a year after delivery), intention of becoming pregnant 7. The receipt of any investigational drug within 12 weeks prior to this trial 8. Previous treatment with liraglutide or sitagliptin 9. The receipt of insulin within 12 weeks prior to this trial (however, a temporary use of no more than 7 days in total within 12 weeks is permitted) 10. Current treatment or expected to start treatment with systemic corticosteroids 11. Any other condition which the attending physician feels would interfere with the trial participation.
研究者
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