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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02870361
Other study ID # 086/2016BO1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2016
Est. completion date April 2018

Study information

Verified date May 2018
Source University Hospital Tuebingen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Insulin resistance is a central pathophysiological component of type 2 diabetes and is associated with a high risk of cardiovascular disease. The tissue in which it manifests are mainly muscle, liver, and adipose tissue. Since the transport of glucose to the brain is independent of insulin, this organ has traditionally not been studied in this regard. In animal experiments, however, knockout of the insulin receptor in the brain leads to obesity and peripheral insulin resistance. This finding of insulin action in the brain could also be confirmed in human studies.

The investigators intend to investigate whether central nervous insulin action affects insulin secretion in humans. For this purpose, nasal insulin and placebo are administered 15 minutes before a hyperglycemic hyperinsulinemic clamps, which stimulate insulin secretion. Insulin sensitivity of the brain is measured by a an established protocol with functional magnetic resonance imaging before and after nasal insulin administration.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date April 2018
Est. primary completion date February 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- HbA1c =6.0%

- normal glucose tolerance during 75g oral glucose tolerance test (OGTT)

Exclusion Criteria:

- Not removable metal parts in or on the body

- manifest cardiovascular disease

- claustrophobia

- recent surgery (less than 3 months)

- Simultaneous participation in other studies

- Acute disease or infection within the last 4 weeks

- neurological and psychiatric disorders

- treatment with centrally acting drugs

- hemoglobin Hb <13g / dl

- Hypersensitivity to any of the substances used

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
intranasal insulin

Placebo


Locations

Country Name City State
Germany University of Tuebingen, Department of Internal Medicine IV Tübingen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Tuebingen

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary Insulin secretion assessed as serum C-peptide levels during a hyperglycemic clamp 0-10 min during hyperglycemic clamp and 10-90 min during hyperglycemic clamp
Secondary Correlation with brain insulin sensitivity Correlation of regional brain insulin sensitivity with the change of pancreatic insulin secretion due to central action of insulin. Changes in regional cerebral blood flow from before to after intranasal insulin administration will be assessed by functional magnetresonance imaging (fMRI) 15-30 minutes post insulin nasal spray
Secondary Differential effects in lean and overweight Differences in the effect of nasal insulin versus placebo on C-peptide levels during a hyperglycemic clamp between lean and overweight men will be assessed. 0-10 min during hyperglycemic clamp and 10-90 min during hyperglycemic clamp
Secondary Correlation with autonomous nervous system activity Correlation of the change in pancreatic insulin secretion by central insulin action with the simultaneous change of the autonomous nervous system (measured by heart rate variability). 10 - 150 minutes post nasal spray
Secondary Peripheral insulin sensitivity Effect of nasal insulin versus placebo on peripheral insulin sensitivity assessed by hyperglycemic hyperinsulinemic clamp. 10-90 min and 70-90 min during hyperglycemic clamp
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