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
| Type | Name | Description |
|---|---|---|
| DRUG | Exenatide | Single subcutaneous injection (10 μg) |
| OTHER | Normal Saline | Single 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.