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An open label,randomized control study for the comparison of pliotropic effects between Glulisine and Glargine with type 2 diabetes

An open label,randomized control study for the comparison of pliotropic effects between Glulisine and Glargine with type 2 diabetes - An open label,randomized control study for the comparison of pliotropic effects between Glulisine and Glargine with type 2 diabetes

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000010353
Enrollment
40
Registered
2014-03-28
Start date
2011-06-01
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 diabetes

Interventions

Insulin glulisine was Administered before every meals. Insulin dose is adjusted every day based on the results of blood glucose self-measurement. insulin glargine was Administered before every sleep

Sponsors

Department of Disease Control and Homeostasis,kanazawa University Graduate School of Medical Science.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The subjects must satisfy the following conditions: 1) An age at the time of obtaining informed consentis more than 20 years old 2) Patients with type 2 diabetes, whose HbA1c is more than 7.4%. 3) Gender is unquestioned: 4) Patients who are admitted to the purpose of glycemic control more than two weeks

Exclusion criteria

Exclusion criteria: 1.Hypersensitivity to components of the insulin glargine and insulin glulisine. 2.None Type 2 diabetes 3.Medical history and/or complication of diabetic ketoacidosis. 4.Medical history and/or complication of severe hypoglycemia. 5.severe infection, around surgery or severe trauma. 6.Patients who received the administration of insulin, DPP-4 inhibitors or GLP-1 analog formulation within 4 weeks. 7.Treatment with glucocorticoid. 8.Uncontrolled Hypertension(systolic blood pressure >160 mmHg or diastolic blood pressure >100 mmHg) 9.Proliferative retinopathy or maculopathy. 10.History of malignancy. 11.Severe health problems not suitable for the study. 12.Patients participated in other clinical trials within one month before the study. 13.Cases that Physicians deem inappropriate as the target of the test.

Design outcomes

Primary

MeasureTime frame
M values

Countries

Japan

Contacts

Public ContactTAKAMURA Toshinari

kanazawa University Graduate School of Medical Science. kanazawa University Graduate School of Medical Science.

ttakamura@m-kanazawa.jp076-265-2234

Outcome results

None listed

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