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The influence of sulfonylurea or dipeptidyl-peptidase-4 inhibitor on glucose control and the secretion of glucagon and insulin induced by sodium glucose transporter-2 inhibitor in type2 diabetic patients

The influence of sulfonylurea or dipeptidyl-peptidase-4 inhibitor on glucose control and the secretion of glucagon and insulin induced by sodium glucose transporter-2 inhibitor in type2 diabetic patients - The influence of sulfonylurea or dipeptidyl-peptidase-4 inhibitor on the secretion of glucagon and insulin induced by sodium glucose transporter-2 inhibitor

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000022661
Enrollment
20
Registered
2016-07-01
Start date
2016-07-01
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

Type2 diabetes mellitus

Interventions

SGLT2i, dapagliflozin 5mg, is administrated once a daily after breakfast during 6-months 3-months after the start of SGLT2i, low dose sulfonylurea, glimeprid 0.5mg, or DPP-4i, linagliptin 5mg, is adde

Sponsors

Chiba Central Medical Center, Diabetes Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with Type2 DM who have been treated on life-style intervension alone and on life-style intervension plus metformin and whose HbA1c have not been controlled under 7.5%

Exclusion criteria

Exclusion criteria: 1. Malignancy 2. Renal dysfunction(eGFR<60ml/min) 3. Liver dysfunction(AST>100U/l and/or ALT100>100U/l), except of fatty liver or non-alcoholic steatohepatitis 4. Pregnancy 5. Lactation 6. History of treatment for ischemic heart disease or other severe cardiovascular disease 7. Administration of any drugs affecting plasma glucose concentration

Design outcomes

Primary

MeasureTime frame
The alternations in glucose and insulin responses after the intravenous glucose load, HbA1c level and fasting glucagon concentration 3 months after administration of SGLT2i and then 3 months after addition of SU or DPP-4i to SGLT2i.

Countries

Japan

Contacts

Public ContactAtsuya Horie

Chiba Central Medical Center Diabetes Center

horie@ccmc.seikei-kai.or.jp043-232-3691

Outcome results

None listed

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