Study for the effects of semaglutide on glycemic control and quality of life in patients with type 2 diabetes
- Conditions
- Type 2 diabetes
- Registration Number
- JPRN-UMIN000042369
- Lead Sponsor
- Hokkaido University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 110
Not provided
1) patients with type 2 diabetes who were treated with GLP-1 receptor agonist other than liraglutide or dulaglutide 2) history of anaphylaxis of semaglutide 3) unstable retinopathy 4) severe hepatic dysfunction or renal dysfunction 5) severe ketosis, diabetic coma 6) severe infection, surgery, serious trauma 7) pregnancy 8) patients who are inadequate to enter this study due to the other reasons by physician's judgments
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The change in HbA1c from baseline at 24 weeks
- Secondary Outcome Measures
Name Time Method 1) The change in QOL scores 2) Adverse effects 3) The change in weight, abdominal circumference, blood pressure and pulse 4) The change in the other blood and urinary tests 5) The factors associated with improvement of HbA1c and secondary endpoints 6) Comparison of the changes between plan A and B when semaglutide demonstrates the superiority compared to both conventional GLP-1 receptor agonists
Related Research Topics
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