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The efficacy of omarigliptin in type 2 diabetic patients

The efficacy of omarigliptin in type 2 diabetic patients - The efficacy of omarigliptin in type 2 diabetic patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000026700
Enrollment
50
Registered
2017-03-28
Start date
2017-03-28
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

None listed

Sponsors

Kawashima Hospital, Social Medical Corporation Kawashima Hospital Group
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Naive cases for DPP-4 inhibitor Patients with poor glycemic control on conventional therapy 2. Additional administration of omarigliptin Patients with poor glycemic control with drug treatment except for DPP-4 inhibitor 3. Cases whose treatment is changed from other DPP-4 inhibitors Criteria of poor glycemic control: HbA1c level exceeding 7.0% and/or glycated albumin level exceeding 21.0%

Exclusion criteria

Exclusion criteria: Patients having infectious diseases, thyroid disease, or malignant tumors. Patients being treated with steroids and changing the dosage. Patients considering not eligible for this trial by attending doctors due to any medical reasons.

Design outcomes

Primary

MeasureTime frame
The change in postprandial plasma glucose, glycated albumin and HbA1c three months after administration of omarigliptin

Secondary

MeasureTime frame
1. Body wight, blood pressure, body composition 2. Serum C peptide 3. Incidence of adverse events 4. Incidence of hypoglycemia 5. Medication adherence, QOL

Countries

Japan

Contacts

Public ContactMachiko Komatsu

Kawashima Hospital, Social Medical Corporation Kawashima Hospital Group Department of diabetes mellitus

machikomatsu@r7.dion.ne.jp088-631-0110

Outcome results

None listed

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