Clinical Trials Directory

Trials / Completed

CompletedNCT03030911

Dexmedetomidine vs Midazolam on Resting Energy Expenditure in Critically Ill Patients

The Effect of Dexmedetomidine vs Midazolam on Resting Energy Expenditure in Critically Ill Patients: Randomized Controlled Study

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to compare the effect of dexmedetomidine on resting energy expenditure in relation to the midazolam in critically ill patients using indirect calorimetry

Detailed description

Caloric needs in critically-ill patients fluctuate significantly over the course of the disease which might expose patients to either malnutrition or overfeeding. Malnutrition is associated with deterioration of lean body mass, poor wound healing, increased risk of nosocomial infection, and weakened respiratory muscles. On the other hand overfeeding in medically compromised patients can promote lipogenesis, hyperglycemia, and exacerbation of respiratory failure. Many factors may affect the resting energy expenditure (REE) through manipulation of oxygen consumption (VO2). Sedatives are important contributors to reduction of REE. The postulated mechanism of sedative-induced reduction of VO2 is inhibition of circulating catecholamine and pro-inflammatory cytokines. Dexmedetomidine is a highly selective α2-adrenoceptor agonist. Stimulation of the α2-adrenoceptor in the central nervous system causes a 60-80% reduction in sympathetic outflow and endogenous catecholamine levels. It was found that perioperative use of α2 agonists decreased sympathetic activity with subsequent reduction of VO2 and REE. Moreover, dexmedetomidine, has some anti-inflammatory effect by inhibiting the pro-inflammatory cytokines which may cause additional reduction of REE in critically ill patient. Midazolam is another important sedative that is frequently used in critically-ill patient. Terao et al. found that increasing the depth of sedation using midazolam, decreased oxygen consumption and REE. However, it remains unclear whether the effect of midazolam on REE is related to the drug itself or to the depth of sedation. There is no direct comparison in the literature between dexmedetomidine and midazolam on REE.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidineThe drug will be administered for sedation and its effect on basal metabolic rate will be investigated
DRUGMidazolamThe drug will be administered for sedation and its effect on basal metabolic rate will be investigated
DRUGFentanylThe drug will be administered in both groups
DEVICEIndirect calorimetryThe device will be used for measurement of basal metabolic rate

Timeline

Start date
2017-01-01
Primary completion
2018-03-10
Completion
2018-03-15
First posted
2017-01-25
Last updated
2018-03-27

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03030911. Inclusion in this directory is not an endorsement.