Type 2 Diabetes Clinical Trial
Official title:
Glimepiride Induced Insulin Secretion Will be Inhibited by Hypoglycemia
This study will look at two FDA approved medications that improve how the pancreas works in patients with Type 2 Diabetes. In order to understand how these medications work in patients with diabetes we must first measure the normal response in healthy volunteers without diabetes. We will be looking at the body's normal physiological response to low blood sugar and whether this will be modified by these medicationsThe hypothesis would be that glimepiride induced insulin secretion will be inhibited by hypoglycemia.
In patients with type 2 diabetes, sulfonylurea drugs are a mainstay for effective glucose
control. These agents produce their hypoglycemic effects via stimulation of endogenous
insulin secretion. Oversecretion of insulin, per se, or a continued relative increase of the
hormone even when plasma glucose is normal will result in hypoglycemia. This latter
situation commonly occurs if a patient decides to omit, delay, or reduce the size of a meal.
An important defense against hypoglycemia in the above situations is glucose dependent
regulation of insulin secretion. In other words, a low ambient glucose concentration could
regulate the magnitude of the amount of insulin released in response to a sulfonylurea. Thus
during hypoglycemic conditions, the sulfonylurea would result in little or no insulin
secretion, whereas its effects during hyperglycemia would be amplified. Glimepiride and
glyburide are both second-generation sulfonlyurea drugs used commonly for treatment of type
2 diabetes. This study will compare the two and ask the following question:
Is Glimepiride insulin secretion dependent upon glucose concentration in-vivo?
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Allocation: Randomized, Intervention Model: Factorial Assignment, Masking: Single Blind (Subject)
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