Type 2 Diabetes Mellitus Clinical Trial
Official title:
The Effects of Insulin Detemir and Gliclazide-MR Treatments in Addition to Life-style Modification and Metformin Therapy on Endothelial Functions in Patients With Type 2 Diabetes : An Open-labelled Randomized Prospective Study
The main purpose of this study is to analyze the effects of the addition of sulfonylurea (gliclazide MR) or ,alternatively, basal insulin (insulin detemir) to life-style modification and metformin treatment as a second step treatment in type 2 diabetes mellitus on endothelial cell functions. The second goal is to identify the effects of these treatment alternatives on body-mass index, the changes in body fat mass, insulin resistance and on the insulin secretion capacity of beta cells. The third aim of this study is to determine the success rates of these treatment alternatives on glycemic control at 6 months follow-up.
The lack of enough number of randomized and controlled studies in the treatment of type 2
diabetes is the most important obstacle in recommending a single-drug or a combination
treatment to the other.
The pleomorphic effects of the treatment choices other than the control of hyperglycemia in
type 2 diabetes are equally important. There is yet a lack of the comparison of different
treatment alternatives found in the treatment algorithms of American Diabetes Association
(ADA) both in terms of the effects on hyperglycemia control as well as other pleomorphic
effects. Some of these pleomorphic effects are the change in body-mass index, insulin
resistance, insulin secretion capacity and the effects on endothelial functions and
coagulation status.
This study is mainly prepared to analyze the effects of the addition of sulfonylurea
(gliclazide MR) or alternatively basal insulin (insulin detemir) to life-style modification
and metformin treatment as a second step treatment in type 2 diabetes mellitus treatment
algorithm on endothelial cell functions. The second goal is to identify the effects of these
treatment alternatives on body-mass index, the changes in body fat mass, insulin resistance
and on the insulin secretion capacity of beta cells. The third aim of this study is to
determine the success rates of these treatment alternatives on glycemic control at 6 months
follow-up. This study in this sense is expected to shed the light on the decision of best
treatment option as well as an essential contribution to the lacking literature in the
field.
To reach these aims, 20-65 year-old patients applying to the endocrinology and the
metabolism outpatient unit, having type 2 diabetes diagnoses with unregulated blood glucose
levels after first step treatment (life-style modification and metformin) will be recruited
and randomized either to the Gliclazide MR arm or the Insulin Detemir arm. As soon as
patients in each arm reach to the target glycemic levels (0. week), basal tests showing
endothelial function as well as inflammatory and coagulation status such as flow-mediated
dilatation (FMD)and investigation of the peripheral blood levels of TNF-α, IL-6, MCP-1,
sICAM-1, sVCAM-1, vWF, E-selectin, P-selectin, endothelin-1, PAI-1, tPA and HMW adiponectin
will be performed. To investigate the insulin resistance and the changes in insulin
secretory capacity of beta cells, mixed meal test will be performed and data obtained about
glucose as well as insulin levels during mixed meal test will be evaluated. To identify the
changes in body-fat mass, bioimpedance analyses will also be performed. All these basal
tests will be repeated in each study subject, 12 weeks and 24 weeks after reaching the
target glycemic levels. Patients randomized to insulin detemir arm in the beginning will
only have gliclazide MR treatment after the 12.week tests are performed. The effects of
continuous gliclazide MR treatment or early insulin detemir followed by gliclazide MR
treatment on endothelial cell functions, inflammation and coagulation, insulin resistance,
insulin secretory capacity of beta cells and body-fat mass will be evaluated by comparing
the 0. week with 12. and 24. week values within each arm as well as 24. week values between
arms.
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Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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