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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00418288
Other study ID # 2005-0089
Secondary ID
Status Completed
Phase N/A
First received January 3, 2007
Last updated June 9, 2008
Start date January 2007
Est. completion date February 2008

Study information

Verified date June 2008
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority Denmark: Ethics Committee
Study type Interventional

Clinical Trial Summary

Type 2 diabetes mellitus, T2D is a disease characterized by an immense growing prevalence world wide with an increased risk of myocardial infarction and stroke. GLP-1 has convincing effects on the high glucose levels in type 2 diabetic patients and is well tolerated. New animal studies indicate a protective effect of GLP-1 in the brain and the heart. The mechanism behind this is yet not known.

The study hypothesis is that during hypoglycaemia GLP-1 will stimulate glucose-uptake in the brain and heart independent of insulin and thereby exert protective effects in the brain.


Description:

Type 2 diabetes mellitus, T2D is a disease characterized by an immense growing prevalence world wide. T2D is associated with a three-fold increase in cardiovascular complications (myocardial infarction and stroke) leading to significantly higher morbidity and mortality in this group of patients. The prospective British Diabetes Study (UKPDS) showed that neither diet alone nor the pharmaceutical treatment utilized (Sulphonylurea, Metformin, Insulin) were able to reduce these macrovascular complications. GLP-1 (glucagon-like-peptide-1)is an incretin with convincing effects on glycaemia in type 2 diabetic patients with little or no risk of hypoglycaemia. New research in animal models has shown a potential protective effect in the brain and heart in association with ischaemic damage. The mechanism behind this protective effect is not known. During hypoglycaemia the brain lacks glucose which is the main fuel for sufficient brain function. The brain will compensate by increasing glucose uptake across the blood brain barrier and similarly in the heart.

The effect of native GLP-1 on glucose uptake in the brain and heart will by visualized by fluoro-deoxy-glucose FDG-PET-scan during hypoglycaemia in healthy men. At the same time a pancreatic/pituitary clamp will be performed. The hypothesis is that GLP-1 directly will stimulate glucose uptake independent of the pancreatic hormones and through this mechanism exert neuro- and cardioprotective actions.

Comparisons: FDG-uptake in the brain and heart with GLP-1 infusion compared to placebo.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date February 2008
Est. primary completion date October 2007
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

- Healthy men

- Age 20-50 years

- Caucasian

- BMI 20-30 kg/m2

Exclusion Criteria:

- Diabetes in subject and 1.degree relatives

- Any disease of clinical relevance

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Intervention

Drug:
glucagon-like-peptide-1
intravenous infusion of 1.2pmol/kg/min for 7 hours
placebo
intravenous infusion of 1.2pmol/kg/min

Locations

Country Name City State
Denmark Department of pharmacology, Aarhus university Aarhus

Sponsors (1)

Lead Sponsor Collaborator
University of Aarhus

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary The acute effect of GLP-1 on glucose uptake in the brain 1 hour
Primary The acute effect of GLP-1 on glucose uptake in the heart 1 hour
Secondary The acute effect of GLP-1 on glucose metabolic rate in the brain 1 hour
Secondary The acute effect of GLP-1 on intracerebral glucose concentration 1 hour
Secondary The acute effect of GLP-1 on lumped constant in the brain 1 hour
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