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临床试验/JPRN-UMIN000021479
JPRN-UMIN000021479已完成4 期

Effect of dapagliflozin, the sodium-glucose-cotransporter-2 (SGLT2) inhibitor, on fibroblast growth factor 21 (FGF21), a novel hepatokine and myokine, in Japanese patients of type 2 diabetes - Effect of dapagliflozin on FGF21.

ational Hospital Organization Kyoto Medical Center0 个研究点目标入组 60 人开始时间: 2016年4月1日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
60

研究概览

简要总结

Bodyweight decreased in the dapagliflozin group, but the changes in SMM were not significant between the groups, thereby elevating the ratio of SMM-to-bodyweight in the dapagliflozin group. Myostatin levels were significantly decreased, and irisin levels showed a nearly significant reduction in the dapagliflozin group compared with the control group, whereas FGF21 levels did not change significantly from baseline to the end of the intervention in both groups.

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • 1.Subjects with secondary obesity associated with endocrine disorders 2.Type 1 diabetes mellitus 3.Subjects with severe ketosis, diabetic coma or precoma 4.Subjects with severe infection, before and after surgery or severe injury 5.Subjects with severe hepatic dysfunction 6.Subjects with moderate or more of renal dysfunction (serum creatinine >= 1.5mg/dl[male], 1.3mg/dl[female]). 7.The subjects within the past 6 months, developed stroke, myocardial infarction, or other serious vascular complications requiring hospitalization 8.Subjects with dehydration, diarrhea, vomiting or gastrointestinal injury 9.Subjects in SGLT-2 inhibitors, insulin formulation, GLP-1 receptor agonist prescription 10.Subjects in TZD, fibrate prescription 11.Subjects in pregnant women, lactating women, the potential or planned are pregnant 12.Subjects with a history of hypersensitivity to SGLT-2 inhibitor 13.Subjects who have been determined to be unsuitable for the attending physician

研究者

发起方
ational Hospital Organization Kyoto Medical Center

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