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Evaluation of efficacy and safety of Alogliptin in type 2 diabetic patients with chronic kidney disease

Evaluation of efficacy and safety of Alogliptin in type 2 diabetic patients with chronic kidney disease - Evaluation of efficacy and safety of Alogliptin in type 2 diabetic patients with chronic kidney disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008133
Enrollment
50
Registered
2012-06-12
Start date
2012-07-01
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

Type 2 Diabetic Patients with chronic kidney Disease

Interventions

Add-on Alogliptin

Sponsors

Department of Internal Medicine, Division of Nephrology, Juntendo University Faculty of Medicine
Lead Sponsor
A Clinic named &#39
Collaborator
Meguro Orthopaedics Surgery Internal Medicine&#39
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Patients with chronic kidney disease 2)Type 2 Diabetic Patients 3)Patient who has not taken DPP-4 inhibitor 4)Patient who is competent to understand the aim of this study and agree on it

Exclusion criteria

Exclusion criteria: 1)Type I and secondary diabetes 2)Severe infectious disease, before or after surgery, and severa trauma 3)Severe liver dysfunction (AST: 100 IU/l or higher) 4)Under treatment with an incretin preparation, such as other DPP-4 inhibitors, at the time of study initiation 5)Pregnant, lactating, and possibly pregnant women and those planning to become pregnant 6)Under treatment with therapeutic drugs not concomitantly administrable with incretin preparations, such as DPP-4 inhibitors, with regard to national health insurance 7)Past medical history of hypersensitivity to alogliptin 8)Judged as ineligible by clinical investigators

Design outcomes

Primary

MeasureTime frame
HbA1c, at-any-time blood sugar level, blood pressure, albuminurina, proteinuria, eGFR at 0, 3, 6 and 12 months after starting of treatment

Secondary

MeasureTime frame
Body weight and side effects

Countries

Japan

Contacts

Public ContactHitoshi Suzuki

Juntendo University Faculty of Medicine Department of Internal Medicine, Division of Nephrology

shitoshi@juntendo.ac.jp03-3813-3111

Outcome results

None listed

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