Recent reports suggest that most beneficial results of glutamine have been obtained with the parenteral administration of high doses of glutamine (0.35 g/Kg/d) and in some special group of patients, such as traumatic patients. Nevertheless total parenteral nutrition is not often used in critically ill patients. The endovenous administration of the the dipeptide N(2)-L-alanyl-L-glutamine in trauma ICU patients can reduce the number of infections, ICU length of stay and mortality. This benefit can be achieved independently the type of nutrition (enteral or parenteral nutrition), being a pharmaconutrient.
Objective: To evaluate the efficacy of the endovenous administration endovenous glutamine to reduce the number of infectious complications, mortality and ICU length of stay in trauma ICU patients. To achieve this objective we have designed this pilot study to obtain the necessary data to design a bigger trial in the future. Other objectives include: * To evaluate the efficacy of glutamine in different patients regarding their severity: patients with an Injury Severity Score\> 25 and patients with lower plasma levels of glutamine. * To registry the possible adverse events of the endovenous administration of glutamine.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
150
0.5 g/kg/day of dipeptide N (2)-L-Alanyl-L-Glutamine
100 mL of physiological serum indistinguishable from active comparator
Hospital Universitario Son Dureta
Palma, Balearic Islands, Spain
RECRUITINGNumber of infections
Based on the results of the ENVIN trial, the median ICU length of stay of trauma patients admitted to the ICU in Spain, is 10 days.
Time frame: ICU discharge (median ten days)
ICU Mortality
Time frame: ICU mortality measured at 1 month after hospital admission
SAfety of endovenous administration
Time frame: 5 days from the beginning of treatment
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.