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临床试验/JPRN-UMIN000006196
JPRN-UMIN000006196招募中未知

evaluation of aloGliptin`s eFficacy and saFety based on Renal function Study - evaluation of aloGliptin`s eFficacy and saFety based on Renal function Study (eGFR Study)

Kansai Electric Power Hospital0 个研究点目标入组 20,000 人开始时间: 2011年8月22日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
20,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Patients meeting one of the following conditions will be excluded: 1) Severe ketosis, diabetic coma or precoma, Type 1 diabetes 2) Severe infectious disease, before or after surgery, and severe trauma 3) Past medical history of hypersensitivity to alogliptin 4) hospitalized patient 5) Pregnant, lactating, and possibly pregnant women and those planning to become pregnant 6) Under treatment with other DPP-4 inhibitors and/or GLP-1 analogues 7) Judged as ineligible by clinical investigators

研究者

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