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Study for the effects of semaglutide on glycemic control and quality of life in patients with type 2 diabetes

Phase 4
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
Inclusion Criteria

Not provided

Exclusion Criteria

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
NameTimeMethod
The change in HbA1c from baseline at 24 weeks
Secondary Outcome Measures
NameTimeMethod
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
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