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临床试验/JPRN-UMIN000007487
JPRN-UMIN000007487招募中4 期

Blood-Glucose reduction in Type 2 Diabetes Patients when using two different DPP-4, alogliptin or sitagliptin during 52-week administration - Blood-Glucose reduction using DPP-4 agents

Biomedis International Ltd Study Management0 个研究点目标入组 300 人开始时间: 2012年3月20日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
300

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
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1. Type 1 diabetes or secondary diabetes 2. Patients with severe infecious disease, operation planned or just after done, and/or serious externalinjyury 3. Other DPP-4 agents users on the enrollement 4. Insulin users 5. Pregnant and possible pregnant, or Lactation 6. AST or ALT 2.5 times or more of normalvalue 7. Serum creatinine2 mg/dL or more 8. Patients with old myocardial infarction, angina pectoris and/or stroke 9. Patients having history of hypersensitivity against study drugs 10.Inappropriate reasons on the enrollment that the physicians/investigators are judged

研究者

发起方
Biomedis International Ltd Study Management

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Blood-Glucose reduction in Type 2 Diabetes Patients... | 临床试验