Diabetes Mellitus Clinical Trial
Official title:
The Effect of Rapid-acting Insulin Injected by Needle-free Jet-injection in the Management of Hyperglycemia in Patients With Diabetes
The purpose of this study is to compare the pharmacokinetic and pharmacodynamic profile of the rapid-acting insulin analogue aspart (Novorapid®) injected subcutaneously by jet-injection to that of the same insulin injected with a conventional pen in the management of hyperglycemia in subjects with diabetes
Recently, we showed in both healthy, non-diabetic volunteers and in patients with type 1
(T1DM) and insulin-treated type 2 diabetes (T2DM) a 40-50% faster absorption of rapid-acting
insulin analogues when administered by jet injection technology rather than by conventional
insulin pen. The faster insulin action of insulin administration by jet injection may be
especially advantageous for correction of hyperglycemia.
To investigate this, a open-label randomised controlled cross-over study will be performed
in 20 adult patients (18-75 years) with T1DM or T2DM on basal-bolus insulin treatment.
The pharmacokinetic and pharmacodynamic profile of insulin aspart will be derived from the
time-action profiles of insulin and glucose, respectively, in response to insulin (in a dose
of 1.5 times the amount of insulin needed to reduce blood glucose to 6 mmol/l calculated by
the insulin-sensitivity factor) after reaching hyperglycemia (18-23 mmol/l). All patients
will be investigated twice, where on one occasion the jet-injector device will be used to
inject insulin, and on the other occasion insulin will be injected with a conventional
insulin pen. The order of these occasions will be randomised. Both devices will be operated
by the patient after sufficient training. Ease of use will be evaluated.
;
Allocation: Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
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