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临床试验/JPRN-UMIN000044264
JPRN-UMIN000044264已完成未知

Comparison of clinical efficacy and safety of weekly GLP-1 receptor agonists dulaglutide and semaglutide - Comparison of clinical efficacy and safety of dulaglutide and semaglutide

Kawasai Medical School0 个研究点目标入组 120 人开始时间: 2021年6月10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
120

研究概览

简要总结

The primary endpoint was the difference of HbA1c level between 2 groups at 24 weeks. The HbA1c level at 24 weeks was significantly lower in S than D. Reduction in BMI and VFA levels were also more significant in S, BMI: 29.2 to 28.8 vs. 29.4 to 28.1

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

  • Type 1 diabetes patient Patients using insulin Patients treated with GLP-1 receptor agonist within 3 months Patients with a history of severe ketosis, diabetic coma, or precoma within the last 6 months Pregnant or potentially pregnant women and lactating patients Diabetic patients with specific mechanisms and diseases (exocrine pancreatic disease, endocrine disease, drug-induced, hereditary) Cases during steroid administration Patients with malignant tumors Patients with severe infections, before and after surgery, and with serious trauma Patients with severe liver damage Other cases judged to be inappropriate

研究者

发起方
Kawasai Medical School

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