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Efficacy and safety of switching from thrice daily glinide or alpha-GI to twice daily mitiglinide/voglibose combined drug in type 2 diabetes.

Efficacy and safety of switching from thrice daily glinide or alpha-GI to twice daily mitiglinide/voglibose combined drug in type 2 diabetes. - Efficacy and safety of switching from thrice daily glinide or alpha-GI to twice daily mitiglinide/voglibose combined drug in type 2 diabetes.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011167
Enrollment
20
Registered
2013-07-18
Start date
2013-07-23
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 diabetes

Interventions

Administration of mitiglinide/voglibose combination (twice daily) Administration of glinide or alpha-GI (thrice daily)

Sponsors

Juntendo University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)The patients treated with diet therapy and glinide or alpha-GI of fixed dosage and administrated for eight weeks or longer before start of observation period. 2)The patients who can take fixed dosage and same medicine during the study, in case of being treated with combination therapy of oral hypoglycemic agents other than glinide or alpha-GI for eight weeks or longer before start of observation period. 3)The patients with HbA1c(NGSP) less than 8.4% (start of observation period and start of treatment period). 4)The patients who can measure SMBG. 5)The patients whose age are more than 20 years. 6)Outpatients.

Exclusion criteria

Exclusion criteria: 1)The patients applicable to the contraindications of mitiglinide or voglibose. 2)The patients who are treated with combination therapy of gulinide and alpha-GI. 3)The patients who has an administration history of SU drug within eight weeks before start of observation period. 4)The patients who drink alcohol too much. 5)The patients complicated with severe diabetic microangiopathy. 6)The patients complicated with severe hepatic diseases or severe renal diseases. 7)The patients complicated with severe cardiac disease. 8)The patients complicated with severe hypertension. 9)The patients who are treated with GLP-1 analog or insulin, or the patients who need their treatment. 10)In addition, the patients whom researchers judged to be inappropriate to study participation.

Design outcomes

Primary

MeasureTime frame
Changes of HbA1c (NGSP) from baseline

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026