Diabetes Clinical Trial
Official title:
An Efficacy and Safety Comparison of Basal Insulin and OADs in Newly Diagnosed Type 2 Diabetes After Short-term Intensive Insulin Therapy
The investigators designed this prospective, randomized control study to compare the efficacy and safety between the basal insulin glargine therapy and metformin-based OADs after correction of the glucose toxicity with a short period of intensive insulin therapy.
Detailed Description:
OBJECTIVE—Type 2 diabetes is associated with defects in insulin secretion and insulin
sensitivity. Hyperglycemia may aggravate these defects, a feature known as glucose toxicity.
Previous studies have shown that acute correction of hyperglycemia in subjects with
long-standing type 2 diabetes gives only short-term improvement in glycemic control after
discontinuation of insulin. The current study attempts to identify whether basal insulin
glargine or metformin-based OADs for further management would have a long-term benefit in
newly diagnosed type 2 diabetes after short-term intensive insulin therapy.
RESEARCH DESIGN AND METHODS—Newly diagnosed type 2 diabetic patients (fasting blood glucose
>200 mg/dL or random blood glucose >300 mg/dL) will be hospitalized and treated with
intensive insulin injection for 10 to 14 days. HbA1c were measured before intensive insulin
injection. After discharge, patients will be randomized to receive basal insulin injection
or metformin-based OADs for further management. Patients will be followed in our clinics and
adjust their medication according to their blood glucose levels. HbA1c were measured 6
months later.After the six-month intervention, these patients were continually followed up
for another six months. Subjects received an oral glucose tolerance test (OGTT) after the
intensive insulin therapy and at the end of the 6th and 12th month.
EXPECTED RESULTS—We will expect that basal insulin glargine,compared with metformin-based
OAD treatment,could more effectively maintain adequate glycemic control in newly diagnosed
type 2 diabetes after short-term intensive insulin therapy.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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