Trials / Terminated
TerminatedNCT00798590
The Efficacy of Glucagon Like Peptide (GLP) - 1(7-36) Amide for Glycemic Control in Critically Ill Patients
The Efficacy of GLP - 1 (7-36) Amide for Glycemic Control in Critically Ill Surgical Patients
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 19 (actual)
- Sponsor
- Johns Hopkins University · Academic / Other
- Sex
- All
- Age
- 21 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this present proposal is to examine the efficacy of GLP-1 administered to control blood glucose in critically ill patients.
Detailed description
All patients whom on admission to the ICU (surgical, burn, \& cardiac) who are expected to receive intensive insulin therapy for at least 72 hours are eligible to be enrolled. Once enrolled, the patients will be randomized to one of two groups: the experimental (intravenous GLP-1 infusion for 72 hours) or control groups (intravenous 0.9% sodium chloride (NaCl) infusion for 72 hours) in a double masked fashion. While enrolled, all patients will receive standard-of-care insulin therapy. Both groups will be maintained on the standard ICU specific protocol for glucose control.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Glucagon-Like Peptide-1 | 5ng/kg-1/min-1 GLP-1 infused in 3 ml continuously over 72 hours. |
| DRUG | Saline | 5ng/kg-1/min-1 placebo infused in 3 ml continuously over 72 hours. |
Timeline
- Start date
- 2008-12-01
- Primary completion
- 2010-06-01
- Completion
- 2011-06-01
- First posted
- 2008-11-26
- Last updated
- 2017-07-02
- Results posted
- 2017-07-02
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00798590. Inclusion in this directory is not an endorsement.