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
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | isoglycemic intravenous glucose infusion and Glucagon infusion, day C | Infusion of 0.8ng/kg/min glucagon from time 0-25min |
| BIOLOGICAL | Oral glucose tolerance test, day A | |
| BIOLOGICAL | intravenous 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.