Clinical Trials Directory

Trials / Completed

CompletedNCT00974272

Effects of Exenatide on Postprandial Hyperlipidemia and Inflammation

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
39 (actual)
Sponsor
Carl T. Hayden VA Medical Center · Federal
Sex
All
Age
35 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The primary goal of this study is to determine the acute effects of exenatide on postprandial hypertriglyceridemia. Secondary goals are to determine whether there are additional improvements in postprandial lipids and lipoproteins and whether (by the reduction of hyperglycemia alone or in combination with declines in hyperlipidemia) exenatide reduces the pro-inflammatory potential of the postprandial period.

Conditions

Interventions

TypeNameDescription
DRUGExenatideSingle subcutaneous injection (10 μg)
OTHERNormal SalineSingle subcutaneous injection

Timeline

Start date
2006-08-01
Primary completion
2008-11-01
Completion
2008-11-01
First posted
2009-09-10
Last updated
2009-09-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00974272. Inclusion in this directory is not an endorsement.

Effects of Exenatide on Postprandial Hyperlipidemia and Inflammation (NCT00974272) · Clinical Trials Directory