Trials / Completed
CompletedNCT00736229
Intravenous Exenatide in Coronary Intensive Care Unit (ICU) Patients
Intensive Exenatide Therapy in Hyperglycemic Patients Admitted to the Coronary Intensive Care Unit
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Saint Luke's Health System · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the efficacy of intravenous Exenatide therapy in hyperglycemic patients admitted to the coronary intensive care unit.
Detailed description
Diabetic patients with acute myocardial infarction (MI) have particularly poor outcomes. Clinical practice guidelines from the American College of Cardiology/American Heart Association for the treatment of patients with acute coronary syndromes call for treatment to achieve preprandial glucose \<110 mg/dL, a maximum daily target \<180 mg/dL, and a post-discharge hemoglobin A1c \<7%. Initiation of aggressive insulin therapy is also warranted to achieve blood glucose \<150 mg/dL during days 0-3 and 80-110 mg/dL when possible thereafter. To date, no studies have been conducted assessing the efficacy of intravenous exenatide administration on achieving glucose lowering in hyperglycemic coronary ICU patients.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Exenatide | 0.05 µg/min bolus of open-label exenatide followed by a constant infusion of 0.025 µg/min for 24-48 hours |
Timeline
- Start date
- 2008-08-01
- Primary completion
- 2011-06-01
- Completion
- 2012-08-01
- First posted
- 2008-08-15
- Last updated
- 2014-11-20
- Results posted
- 2014-11-20
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00736229. Inclusion in this directory is not an endorsement.