Clinical Trials Directory

Trials / Completed

CompletedNCT02010827

Endogenous Glucoseproduction in Patients With Type 2 Diabetes Mellitus During Oral Glucose and iv. Glucose Infusion

Status
Completed
Phase
Study type
Observational
Enrollment
20 (actual)
Sponsor
University Hospital, Gentofte, Copenhagen · Academic / Other
Sex
All
Age
35 Years – 80 Years
Healthy volunteers
Accepted

Summary

We want to investigate how lack of glucagon suppression during an oral glucose tolerance test in patients with type 2 diabetes contributes to patients postprandial hyperglycemia.

Detailed description

Patients with type 2 diabetes mellitus (T2DM) are not able to suppress their glucagon secretion after a meal or after ingestion of glucose. Previous studies have shown that gastrointestinal hormones might play a role in this phenomenon. However, it has not yet been possible to determine whether this lack of glucagon suppression postprandially results in an increased endogenous glucose secretion, and thus is a factor in the patients postprandial hyperglycemia. We aim to perform oral glucose tolerance tests and isoglycemic intravenous glucose infusions with and without a continuous glucagon infusion in patients with T2DM and healthy control subjects. The glucagon infusion is aiming at copying the inappropriate "physiological" glucagon response observed in patients with T2DM.

Conditions

Interventions

TypeNameDescription
BIOLOGICALisoglycemic intravenous glucose infusion and Glucagon infusion, day CInfusion of 0.8ng/kg/min glucagon from time 0-25min
BIOLOGICALOral glucose tolerance test, day A
BIOLOGICALintravenous iv glucose infusion, day B

Timeline

Start date
2013-11-01
Primary completion
2014-09-01
Completion
2015-08-01
First posted
2013-12-13
Last updated
2015-12-02

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT02010827. Inclusion in this directory is not an endorsement.