Nippon Ultra-Rapid Insulin and Diabetic Complication Evaluation-Study (NICE-Study)

Diabetes Mellitus Clinical Trial

Official title:

To Investigate Whether the Postprandial Blood Sugar Level as Achieved Using Ultrarapid-Acting Type Insulin Could Prevent Great Vessel Disorder in Japanese Type 2 Diabetic Patients.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00575172
• Other study ID #: UMIN0949
• Secondary ID: UMIN00000949
• Status: Completed
• Phase: N/A
• First received: December 17, 2007
• Last updated: January 7, 2008
• Start date: March 2003
• Est. completion date: December 2007

Study information

• Verified date: December 2007
• Source: Osaka Saiseikai Nakatsu Hospital
• Contact: n/a
• Is FDA regulated: No
• Health authority: Japan: Pharmaceuticals and Medical Devices Agency
• Study type: Observational

Clinical Trial Summary

For the purpose of comparing efficacy of intensive therapy between 1) ultrarapid-acting type insulin (insulin aspart) and 2) conventional rapid-acting type insulin (R), a Multicenter Open Label Randomized Controlled Trial was planned in Japan using the occurrence of cardiovascular events in patients with diabetes, a high risk factor, as an index.

Description:

A survey shows that the most frequently observed direct cause of death in diabetic patients is cardiovascular disorder. However, investigations and surveys such as DCCT, UKPDS and KUMAMOTO-study, etc. clarified that strict control of blood sugar level prevented development and progress of diabetic microangiopathy, but could not show a significant effect on great vessel disorder. Recently, the DECODA-study, DECODE-study and Honolulu-study have demonstrated that postprandial high blood sugar is involved in great vessel disorder. Therefore, possible prevention of great vessel disorder in diabetic patients is suggested by improving the postprandial blood sugar level as achieved using ultrarapid-acting type insulin, which has become available recently. Even with results in Europe and the US obtained, the life-style and incidence of complications in Japanese people are different, and there are many points that remain uncertain with respect to the direct application of foreign results to Japanese people. Therefore, in Japan also, it is necessary to conduct a large-scale clinical study and to establish high-level evidence using mainly Japanese people through hospitals having many patients.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 346
• Est. completion date: December 2007
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 20 Years to 85 Years

Eligibility

Inclusion Criteria:

• Subjects are patients satisfying the following conditions 1) - 3).

1. Outpatients and inpatients aged 20 years or more but younger than 85 years. Men or women.

2. Patients with type 2 diabetes based on the diagnostic standard of the Japanese Diabetes Society

3. No specific restriction on the current treatment. Patients having switched treatment are also accepted.

Exclusion Criteria:

1. Patients with type 1 diabetes

2. Patients with a past history of cerebral angiopathy (cerebral hemorrhage, cerebral infarction, transient cerebral ischemic attack, subarachnoid hemorrhage, etc.) within 6 months before giving consent

3. Patients with a past history of myocardial infarction within 6 months before giving consent

4. Patients planning to receive PTCA or CABG, or who had PTCA or CABG within 6 months before giving consent

5. Patients with coronary arteriopathy (angina pectoris, etc.) that requires treatment with ß-blocker or calcium-antagonist

6. Patients with atrial fibrillation or atrial flutter

7. Patients with renal dysfunction (serum creatinine = 3.0 mg/dL)

8. Patients with liver dysfunction (AST, ALT = 100 IU/L)

9. Patients with a past history or suspected of having a malignant tumor within 5 years before giving consent

10. Pregnant or possibly pregnant patients

11. Other patients judged inappropriate for the study by the investigators (patients presenting difficulty in frequently receiving rapid-acting type insulin or ultrarapid-acting type insulin therapy, including patients' compliance with treatment)

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Diabetes Mellitus

Locations

Country	Name	City	State
Japan	Osaka Saiseikai Nakatsu Hospital	Osaka

Sponsors (1)

Lead Sponsor	Collaborator
Osaka Saiseikai Nakatsu Hospital

Country where clinical trial is conducted

Japan, 

References & Publications (1)

Nishimura H, Shintani M, Kouji M and Nice-study group J Saiseikai Nakatsu Hospital, 20, 216-220, 2003

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cardiovascular events 1)Sudden death 2)New development or recurrence of apoplexy or TIA 3)New development or recurrence of AMI or and angina pectoris 4)Newly developed ASO, amputation of leg due to ASO		five years	Yes
Secondary	1)Total mortality 2)Changes in the mean IMT of common carotid arteries 3)Changes in the pulse wave velocity (PWV) (rt & 1t baPWV), ABI		five years	Yes