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Pharmacology of Insulin Injected With Jet-injection in Diabetes

Phase 4
Completed
Conditions
Diabetes Mellitus
Interventions
Device: jet injection device
Registration Number
NCT01438632
Lead Sponsor
Radboud University Medical Center
Brief Summary

A previous study showed that absorption and glucose-lowering action of rapid-acting insulin analogues occurred twice as fast when these analogues were administered by jet injection technology rather than by conventional insulin pen in healthy non-diabetic subjects. This study investigates if the rapid-acting insulin analogue aspart (Novorapid®) injected with jet-injection or a conventional insulin pen prior to a standardised meal in patients with diabetes shows the same difference in the pharmacokinetic and pharmacodynamic profile.

Detailed Description

A previous study showed that absorption and glucose-lowering action of rapid-acting insulin analogues occurred twice as fast when these analogues were administered by jet injection technology rather than by conventional insulin pen in healthy non-diabetic subjects. This study investigates if the rapid-acting insulin analogue aspart (Novorapid®) injected with jet-injection or a conventional insulin pen prior to a standardised meal in patients with diabetes (type 1 and type 2) shows the same difference in the pharmacokinetic and pharmacodynamic profile.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 injected directly prior to a standardised meal. All patients will be investigated twice, where on one occasion the jet-injector device will be used to inject an individualised dose of insulin and a conventional insulin pen to inject a placebo solution, and on the other occasion insulin will be injected with the conventional pen and placebo with the jet-injector. The order of these occasions will be randomised and blinded to both the investigator and the participating patient. The primary endpoint is the hyperglycaemic burden as reflected by area under the baseline-subtracted plasma glucose concentration time-curve from time 0 to 2 h after insulin injection and meal ingestion (BG-AUC0-2h). Secondary study endpoints are the area under the baseline-subtracted plasma glucose concentration time-curve from time 0 to 6 h (BG-AUC0-6h), maximal glucose excursion (BGmax), time to maximal glucose excursion (T-BGmax), time until plasma glucose has returned to baseline (T-BGBL), maximal insulin concentration (C-INSmax), time to maximal insulin concentration (T-INSmax), area under the insulin concentration curve (INSAUC) and time until 50% of insulin absorption (T-INSAUC50%) after insulin injection and meal ingestion.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
24
Inclusion Criteria
  • Body-mass index 18-32 kg/m2
  • Stable glycaemic control with HbA1c 6.0-9.0%
  • Duration of diabetes >1 year
  • Insulin use at least once daily or with subcutaneous pump
  • Blood pressure <160/90 mmHg
Exclusion Criteria
  • Inability to provide informed consent
  • Requirement of <8 units of rapid-acting insulin (analogue) before meals
  • Chronic use of sulphonylurea derivatives, GLP-1 based treatments, acarbose or thiazolidinediones
  • Treatment with prednisolone, non-steroidal anti-inflammatory drugs (NSAIDs), immunosuppressive agents, cytostatic drugs, hormone therapy except insulin, thyroid supplementation and oral anticonceptives
  • Known allergy to aspart insulin
  • Symptomatic diabetic neuropathy
  • History of a major cardiovascular disease event (myocardial infarction, stroke, symptomatic peripheral artery disease, coronary bypass surgery, percutaneous coronary or peripheral artery angioplasty) in the past 6 months
  • Pregnancy or the intention to become pregnant

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
conventional insulin penjet injection device-
jet injectorjet injection deviceJet injectors deliver insulin at a high velocity (typically \>100m/s) across the skin in the subcutaneous tissue, without the use of a needle
Primary Outcome Measures
NameTimeMethod
BG-AUC0-2h (mmol•min-1•l-1): area under the baseline-subtracted plasma glucose concentration time-curve from time 0 to 2 h after insulin injection and meal ingestion.2 days (2 hours per day)

based on plasma glucose levels during the first two hours of the 6-hour post-meal study duration

Secondary Outcome Measures
NameTimeMethod
BGmax (mmol/l): maximal glucose excursion after insulin injection and meal ingestion2 days (6 hours each day)

Maximal plasma glucose value after the standardised meal

T-BGmax (min): time to maximal glucose excursion after insulin injection and meal ingestion2 days (6 hours per day)

Time until maximal glucose value after the standardised meal and insulin injection

BG-AUC0-6h (mmol•min-1•l-1): area under the baseline-subtracted plasma glucose concentration time-curve from time 0 to 6 h after insulin injection and meal ingestion2 days (6 hours each day)

Based on glucose concentration measurements for the total 6 hours of the study

T-BGBL (min): time until plasma glucose has returned to baseline values after insulin injection and meal ingestion2 days (6 hours per day)

based on glucose level measurements during the total 6 hours of the study

T-INSmax (min): time to maximal insulin concentration (C-INSmax)2 days (6 hours per day)

Maximal insulin concentration after insulin injection

INSAUC (pmol•min-1•l-1): area under the insulin concentration curve (from timepoint 0)2 days (6 hours per day)

Based on insulin concentration measurements during the total 6 hours of the study

T-INSAUC50% (min): time until 50% of insulin absorption (mean residence time, MRT)2 days (6 hours each day)

Based on insulin concentration measurements during the total 6 hours of the study

Number of patients requiring exogenous glucose infusion to prevent postprandial hypoglycaemia after insulin injection and meal ingestion2 days

This will be assessed for the individual patient after every test. After completion of the experiments all cases of hypoglycemia will be assessed

Amount of exogenous glucose required to prevent postprandial hypoglycaemia after insulin injection and meal ingestion2 days

This will be assessed for the individual patient after every test. After completion of the experiments the total amount of glucose infused will be calculate for each device

Duration of time that exogenous glucose is required to prevent postprandial hypoglycaemia after insulin injection and meal ingestion2 days

This will be assessed for the individual patient after every test. After completion of the experiments the total amount of time will be calculate for each device

BG-AUC0-1h2 days (6 hours per day)

the area under the baseline-subtracted plasma glucose concentration time-curve during the first hour

Trial Locations

Locations (1)

Department of general internal medicine 463, section Diabetes, Radboud University Nijmegen Medical Centre

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Nijmegen, Gelderland, Netherlands

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