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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00474838
Other study ID # KIIT-KMC-0701
Secondary ID
Status Completed
Phase Phase 4
First received May 16, 2007
Last updated September 25, 2013
Start date April 2007
Est. completion date December 2012

Study information

Verified date September 2013
Source Kyunghee University Medical Center
Contact n/a
Is FDA regulated No
Health authority Korea: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This randomized controlled prospective study aims to evaluate the efficacy of intensive insulin therapy for long term glycemic control and improvement or preservation of beta cell function in newly diagnosed type 2 diabetes patients.


Description:

Type 2 diabetes is associated with beta cell dysfunction and insulin action at diagnosis of diabetes. Although the relative importance of these two alterations is controversial, growing evidence is swinging to the concept that there is no hyperglycemia without β-cell dysfunction. Also there is agreement that deterioration of glucose tolerance over time is associated with a progressive decrease of beta cell function.

Beside the role of genetic factor, the continuous decline in β-cell function is affected by glucotoxicity generated by hyperglycemia and lipotoxicity due to high fatty acid. A vicious cycle of hyperglycemia per se further impairs and may destroy β-cell. Recently, many reports have shown that early intensive glycemic control plays a role in the prevention of progressive ß-cell function and worsening of diabetes.

Some studies have shown that early intensive insulin therapy(IIT) to achieve near normoglycemia in new onset type 2 diabetes gives short term and long term improvement in glycemic control after discontinuation of insulin. It is suggested that long term glycemic control is associated with improvement of β-cell function.

In the unpublished previous pilot study, the investigators found that early intensive insulin therapy using multiple daily injection (MDI) or daily twice injection in newly diagnosed type 2 diabetes can significantly improve the beta cell function and facilitate further long term glycemic control. To establish the effectiveness of intensive insulin therapy for long term glycemic control and improvement of β-cell function, the investigators will perform a randomized controlled prospective study in newly diagnosed type 2 diabetes in Korea.


Recruitment information / eligibility

Status Completed
Enrollment 112
Est. completion date December 2012
Est. primary completion date August 2012
Accepts healthy volunteers No
Gender Both
Age group 25 Years to 70 Years
Eligibility Inclusion Criteria:

- Newly diagnosed drug naïve type 2 diabetic patient with typical diabetic symptom (polydipsia, polyuria, unexplained weight loss) within recent 1 year

- Initial HbA1c : 8.0 % = HbA1c < 12.0%

Exclusion Criteria:

- Known contraindication to insulin glargine, insulin glulisine, metformin, glimepiride

- Patients with proliferative diabetic retinopathy

- Severe liver disease or AST, ALT = 2.5 x ULN

- History of lactic acidosis

- Unstable or severe angina

- Congestive heart failure

- Chronic disease treated with continuous corticosteroid therapy

- Diagnosis of cancer

- Positive urine pregnancy test or plan to become pregnant during the clinical trial

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
intensive insulin group
Once daily long acting insulin and preprandial rapid acting insulin injection
Oral AntiDiabetic Drug (glimepiride and metformin)
glimepiride and metformin combined therapy

Locations

Country Name City State
Korea, Republic of The Catholic University of Korea Bucheon St.Mary's Hospital Bucheon
Korea, Republic of Inha University Hospital In Cheon
Korea, Republic of Jeju National University Hospital Jeju-do
Korea, Republic of Hanyang University Medical Center Kuri Kyunggi-do
Korea, Republic of Korea University Guro Hospital Seoul
Korea, Republic of Kyung Hee University East Weast Neo Medicalcenter Seoul
Korea, Republic of Kyunghee University Medical Center Seoul
Korea, Republic of Ajou University Medical Center Suwon

Sponsors (9)

Lead Sponsor Collaborator
Kyunghee University Medical Center Ajou University, East West Neo Medical Center, Hanyang University, Inha University Hospital, Jeju National University Hospital, Korea University Guro Hospital, Sanofi, The Catholic University of Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Long-term glycemic control up to 2 years No
Primary Change of pancreatic beta cell function up to 2 years No
Secondary Inflammatory marker and insulin sensitivity up to 2 years No
Secondary Time to reach target goal of blood glucose level up to 2 year No
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