Efficacy and Mechanisms of GLN Dipeptide in the SICU

PHASE3CompletedINTERVENTIONAL
Enrollment

150

Participants

Timeline

Start Date

September 30, 2006

Primary Completion Date

December 31, 2012

Study Completion Date

December 31, 2012

Conditions
Critical Illness
Interventions
DRUG

Glutamine dipeptide with 15% Clinisol

Subjects randomized to AG-PN will receive PN containing 0.5 g/kg/day of L alanyl L GLN (AG) dipeptide (Dipeptiven 20%; Fresenius-Kabi) and 1.0 g/kg/day of 15% Clinisol (Baxter Inc., Deerfield, IL) AA solution (total = 1.5 g/kg/day, with AG replacing 1/3 of Clinisol AA). The amount of GLN dipeptide administered each day will be determined by daily PN volume intake data.

DRUG

15% Clinisol

Subjects randomized to STD-PN will receive 1.5 g/kg/day of 15% Clinisol. The amount of Clinisol administered each day will be determined by daily PN volume intake data.

Trial Locations (5)

30322

Emory University, Atlanta

53792

University Of Wisconsin Hospital, Madison

80262

University of Colorado Health Sciences Center, Denver

02906

The Miriam Hospital/Brown University, Providence

37212-2713

Vanderbilt University, Nashville

All Listed Sponsors
collaborator

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

NIH

lead

Emory University

OTHER

NCT00248638 - Efficacy and Mechanisms of GLN Dipeptide in the SICU | Biotech Hunter | Biotech Hunter