ClinicalTrials.gov
 Home    Search    Study Topics    Glossary  
 

  Full Text View  
  Tabular View  
  Contacts and Locations  
  Related Studies  
Nippon Ultra-Rapid Insulin and Diabetic Complication Evaluation-Study (NICE-Study)

This study has been completed.

Sponsored by: Osaka Saiseikai Nakatsu Hospital
Information provided by: Osaka Saiseikai Nakatsu Hospital
ClinicalTrials.gov Identifier: NCT00575172
  Purpose

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.


Condition
Diabetes Mellitus

MedlinePlus related topics:   Diabetes    Diabetes Complications   

ChemIDplus related topics:   Insulin   

U.S. FDA Resources

Study Type:   Observational
Study Design:   Cohort, Prospective
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.

Further study details as provided by Osaka Saiseikai Nakatsu Hospital:

Primary Outcome Measures:
  • 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 [ Time Frame: five years ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • 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 [ Time Frame: five years ] [ Designated as safety issue: Yes ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Enrollment:   346
Study Start Date:   March 2003
Study Completion Date:   December 2007

Groups/Cohorts
U
Intensified insulin therapy with ultrarapid insulin-analogue (Insulin-Aspart)
R
Intensified insulin therapy with human regular insulin

Detailed 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.

  Eligibility
Ages Eligible for Study:   20 Years to 85 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample

Study Population

Japanese outpatients and inpatients aged 20 years or more but younger than 85 years. Men or women. Patients with type 2 diabetes based on the diagnostic standard of the Japanese Diabetes Society/American Diabetes Association. No specific restriction on the current treatment. Patients having switched treatment are also accepted.


Criteria

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 β-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)
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00575172

Locations
Japan
Osaka Saiseikai Nakatsu Hospital    
      Osaka, Japan, 503-0012

Sponsors and Collaborators
Osaka Saiseikai Nakatsu Hospital

Investigators
Study Chair:     Hideshi Kuzuya, M.D.,Ph.D     Higasiyama Takeda Hospital    
Study Director:     Makoto Otoshi, MD.,Ph.D.     Ohtoshi Clinic    
Principal Investigator:     Haruo Nishimura, MD.,Ph.D.     Osaka Saiseikai Nakatsu Hospital    
Principal Investigator:     Koji Maeda, MD.     Maeda Clinic    
Principal Investigator:     Mitsuyo Shintani, MD.,Ph.D.     Osaka Saiseikai Nakatsu Hospital    
  More Information

NICE-study Homepage  This link exits the ClinicalTrials.gov site
 

Responsible Party:   NICE-study EBM center ( Osaka Saiseikai Nakatsu Hospital )
Study ID Numbers:   UMIN0949, UMIN00000949
First Received:   December 17, 2007
Last Updated:   January 7, 2008
ClinicalTrials.gov Identifier:   NCT00575172
Health Authority:   Japan: Pharmaceuticals and Medical Devices Agency

Keywords provided by Osaka Saiseikai Nakatsu Hospital:
type2 diabetes mellitus  
cardiovascular disease  
macrovascular event  

Study placed in the following topic categories:
Metabolic Diseases
Diabetes Mellitus, Type 2
Diabetes Mellitus
Endocrine System Diseases
Endocrinopathy
Metabolic disorder
Glucose Metabolism Disorders
Insulin
Diabetes Complications

ClinicalTrials.gov processed this record on July 18, 2008




Links to all studies - primarily for crawlers