Clinical Trials Directory

Trials / Completed

CompletedNCT01347801

Mechanisms of Insulin Resistance in Critical Illness: Role of Systemic Inflammation and GLP-1

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Rigshospitalet, Denmark · Academic / Other
Sex
Male
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine the role of inflammation and the insulin regulating hormone GLP-1 during critical illness.

Detailed description

Critically ill patients often exhibit hyperglycaemia. Although the cause of this hyperglycaemia is probably multifactorial, peripheral insulin resistance is a major contributor, similar to type 2 diabetes mellitus (T2D). There are several similarities between critical illness and T2D, including the presence of systemic inflammation and increased plasma free fatty acids (FFA), all of which may induce insulin resistance in healthy volunteers. In critical illness, elevated catecholamines, cortisol, growth hormone and glucagon may also contribute to insulin resistance. The degree of hyperglycaemia correlates with mortality in ICU patients. van den Berghe et al. found that IV infusion of insulin to obtain strict normoglycaemia reduced mortality as well as morbidity in critically ill surgical patients and in some medical ICU patients. However, insulin increases the risk of hypoglycaemia; this is a major obstacle to strict euglycaemia in ICU patients and may explain the inability of others to reproduce the benefits reported by van den Berghe et al. Thus, alternatives to insulin for controlling plasma glucose (PG) in ICU patients are warranted. Aim: To study the role of the incretin hormone, glucagon-like peptide (GLP)-1 for glycaemic, metabolic, hormonal and inflammatory profile in * critically ill patients in the intensive care unit (ICU) and * healthy volunteers exposed to a standardised systemic inflammation

Conditions

Interventions

TypeNameDescription
DRUGGLP-1GLP-1 1,2pmol/kg/min i.v. infusion for 4 hours
DRUGPlacebo (Saline)Normal saline (NaCl 0,9%)
DRUGTNF-alfa1000ng/m2 BSA/hour i.v. infusion for 4-6 hours
OTHEROGTTOral glucose tolerance test with 75 g glucose
OTHERIVGTTIntravenous glucose tolerance test with infusion of 20% glucose matching the glucose profile of the corresponding OGTT

Timeline

Start date
2011-03-01
Primary completion
2014-09-01
Completion
2014-09-01
First posted
2011-05-04
Last updated
2014-09-22

Locations

2 sites across 1 country: Denmark

Source: ClinicalTrials.gov record NCT01347801. Inclusion in this directory is not an endorsement.