Clinical Trials Directory

Trials / Completed

CompletedNCT00784745

Is Insulin Resistance and/or Glucose Intolerance Pathogenetic in the Development of a Reduced Incretin Effect

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
21 (actual)
Sponsor
University Hospital, Gentofte, Copenhagen · Academic / Other
Sex
All
Age
20 Years – 70 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to examine whether there is a causal relationship between insulin resistance and/or glucose intolerance in the development of a defect incretin effect.

Detailed description

In this study we are going to examine the incretin effect before and after the development of insulin resistance and/or glucose intolerance. The incretin effect is the increased insulin response seen after an oral as apposed to an intravenous glucose challenge with identical plasma glucose profiles. This insulin enhancing effect is greatly reduced in type 2 diabetes. Since the development of type 2 diabetes is preceded by insulin resistance and glucose intolerance we wanted to examine the incretin effect in the early stages of type 2 diabetes. To do this, we want to induce insulin resistance and/or glucose intolerance. This is achieved by 5 days of treatment with dexamethasone. The incretin effect in this study will be examined by 3 investigations prior to the treatment and 3 days following the treatment. Day 1: Oral glucose challenge with 75 g of glucose. The subject is asked to drink 75g of glucose suspended in 300mL of water. During the 4 hours of the test, we draw blood at various times during the study to determine the concentration of: Glucose, GLP-1, GIP, Glucagon, Insulin and c-peptide. Day 2: Intravenous glucose We duplicate the glucose curve obtained from day 1. We also draw blood during this test to the same end as in day 1. Day 3: Mixed meal. The subjects are served a mixed meal. During this 4 hour test, we draw blood to examine the response to a standardized meal. The test involves sampling blood as described for the other days.

Conditions

Interventions

TypeNameDescription
DRUGDexamethasone2mg morning and night for 5 days.

Timeline

Start date
2008-11-01
Primary completion
2009-08-01
Completion
2009-09-01
First posted
2008-11-04
Last updated
2014-05-21

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00784745. Inclusion in this directory is not an endorsement.