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Effect of Rosiglitazone on ADMA in Critical Illness

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00409097
Enrollment
30
Registered
2006-12-08
Start date
2006-04-30
Completion date
2007-12-31
Last updated
2006-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critical Illness, Multiple Organ Failure

Keywords

ADMA, MOF, Critical illness

Brief 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.

Interventions

DRUGRosiglitazone

Sponsors

Amsterdam UMC, location VUmc
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* critically ill patients * age between 18 and 75 years * SOFA score \> 7

Exclusion criteria

* history of Diabetes mellitus * history of hypercholesterolemia * history of hyperhomocysteinemia * impaired hepatic function

Design outcomes

Primary

MeasureTime frame
ADMA concentration

Secondary

MeasureTime frame
SOFA score
Organ function
Mortality

Countries

Netherlands

Contacts

Primary ContactMilan C Richir, MD
m.richir@vumc.nl0031 20 4443601

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026