Clinical Trials Directory

Trials / Unknown

UnknownNCT00409097

Effect of Rosiglitazone on ADMA in Critical Illness

Status
Unknown
Phase
Phase 3
Study type
Interventional
Enrollment
30 (planned)
Sponsor
Amsterdam UMC, location VUmc · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether Rosiglitazone,decreases the ADMA concentration and thereby increases the arginine/ADMA ratio of critically ill patients.

Detailed description

Endothelial vasodilatation dysfunction precedes the development of arteriosclerosis. The endothelium plays a pivotal role in the control of the vascular tone by releasing nitric oxide (NO). The amino acid arginine is the sole substrate for the enzyme NO synthase (NOS). Asymmetric dimethylarginine (ADMA) is an endogenous derivative of arginine that inhibits NOS. Thus the arginine/ADMA ratio an important determinant of NO production by NOS. ADMA is an independent risk factor for cardiovascular disease, but elevated levels of ADMA have also been shown to be a strong independent predictor of ICU mortality. The central mechanism by which ADMA may cause deterioration in critically ill patients is by impairing organ blood flow and reducing cardiac function, especially during stress. Accumulation of ADMA could thereby be a causative factor in the development multi organ failure (MOF). Thus inhibition of NO production by ADMA may become especially important when cardiac demand is increased.

Conditions

Interventions

TypeNameDescription
DRUGRosiglitazone

Timeline

Start date
2006-04-01
Completion
2007-12-01
First posted
2006-12-08
Last updated
2006-12-08

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00409097. Inclusion in this directory is not an endorsement.