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Effect of gulcose-lowering agents on adipocytokine levels in patients with diabetes mellitus

Effect of gulcose-lowering agents on adipocytokine levels in patients with diabetes mellitus - Comparative study of ipragliflozin versus metformin on adipocytokine levels

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000017113
Enrollment
30
Registered
2015-05-26
Start date
2015-03-01
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

type 2 diabetic patients with coronary artery disease

Interventions

group A: additive therapy of ipragliflozin 50-100mg once daily to DPP4 inhibitor for 6 months Group B: additive therapy of metformin 250-750mg twice daily to DPP4 inhibitor for 6 months

Sponsors

Anjo Kosei Hospital, Cardiovascular Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who have a history of following coronary heart diseasese CABG or PCI was performed more than 6 months before >= 50% coronary artery stenosis according to the ACC/AHA classification was found by CAG 2) Diabetic patients under treatment of DPP-4 inhibitor more than 3 months 3) Patients who are judged to require the more glucose-lowering therapy

Exclusion criteria

Exclusion criteria: 1) Patients with malignancy 2) Patients with history of hypersensitivity against DPP4 inhibitor, SGLT2 inhibitor, and biguanide drugs 3) patients whose glycemic control is extremely poor (HbA1c >=10%) 4) patients whose glycemic control is very poor (HbA1c >=10%) 5) Pregnant women, women who may be pregnant, and breast-feeding women. 6) Patients with history of renal transplantation, urinary infection, sexually transmission disease, and non-cardiogenic stroke 7) Patients who took diuretics 8) patients whose BMI is lower than 18.5 9) Patients with history of acute coronary syndrome within 6 months 10) Patients judged by the investigator/ sub investigator to be ineligible for some other reason

Design outcomes

Primary

MeasureTime frame
Changes in adipocytokine

Secondary

MeasureTime frame
Changes in glucose metabolism Changes in body weight and abdominal circumference Changes in laboratory parameters Assessment of vascular event

Countries

Japan

Contacts

Public ContactYusuke Uemura

Anjo Kosei Hospital cardiovascular Center

yusuke0307@hotmail.com0566-75-2111

Outcome results

None listed

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