Clinical Trials Directory

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

TypeNameDescription
DRUGGlucagon-Like Peptide-15ng/kg-1/min-1 GLP-1 infused in 3 ml continuously over 72 hours.
DRUGSaline5ng/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.