Skip to content

Evaluation of the influence of Vildagliptin on chorioretinal blood flow in patients with diabetic retinopathy

Evaluation of the influence of Vildagliptin on chorioretinal blood flow in patients with diabetic retinopathy - Evaluation of the influence of Vildagliptin on chorioretinal blood flow in patients with diabetic retinopathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009641
Enrollment
50
Registered
2012-12-31
Start date
2013-01-01
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

diabetic retinopathy

Interventions

Add each treatment for 6 months. 1) vildagliptin 50 or 100mg/day 2) other oral hypoglycemic drugs except anti-dipeptidyl peptidase-4 (DDP-4) inhibitor

Sponsors

Nagasaki University Graduate School of Biomedical Sciences
Lead Sponsor
1. Department of Metabolism/Diabetes and Clinical Nutrition, Nagasaki University Hospital 2. Department of Ophthalmology, Nagasaki University Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Type 2 diabetic patients who meet the following requirements 1) Diabetic retinopathy requiring treatment 2) 6.9%<=HbA1c<=11.0% 3) No prior treatment using DDP-4 inhibitor 4) No change of oral hypoglycemic drugs for 3 months prior 2. Patients over 20 years-old. 3. Patients who have been informed and have understood the full explanation of this study, and have agreed and given prior written consent.

Exclusion criteria

Exclusion criteria: 1. Type 1 diabetes, diabetic ketoacidosis or diabetic coma 2. Severe liver or kidney dysfunction 3. Severe infection or traumatic injury 4. In a perioperative period of major surgery 5. Anti-glutamic acid decarboxylase (GAD) antibody>=10U/ml 6. Poorly controlled hypertension; systolic blood pressure>=160mmHg or diastolic blood pressure>=100mmHg 7. Pregnant female, female with possibility of pregnancy and breast-feeding female 8. History of hypersensitivity to targeted medication 9. History of severe cardiovascular or cerebrovascular disease in 6 months 10. Any other factors that may disqualify the patient

Design outcomes

Primary

MeasureTime frame
chorioretinal blood flow

Secondary

MeasureTime frame
best corrected visual acuity, intraocular pressure, central retinal thickness, HbA1c, fasting blood glucose

Countries

Japan

Contacts

Public ContactYuki Maekawa

Nagasaki University Graduate School of Biomedical Sciences Department of Ophthalmology & Visual Sciences

maekaway@nagasaki-u.ac.jp095-819-7345

Outcome results

None listed

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