search
Back to results

Effect of Rosiglitazone on ADMA in Critical Illness

Primary Purpose

Critical Illness, Multiple Organ Failure

Status
Unknown status
Phase
Phase 3
Locations
Netherlands
Study Type
Interventional
Intervention
Rosiglitazone
Sponsored by
Amsterdam UMC, location VUmc
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Critical Illness focused on measuring ADMA, MOF, Critical illness

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • VU University Medical CenterRecruiting

Outcomes

Primary Outcome Measures

ADMA concentration

Secondary Outcome Measures

SOFA score
Organ function
Mortality

Full Information

First Posted
December 7, 2006
Last Updated
December 7, 2006
Sponsor
Amsterdam UMC, location VUmc
search

1. Study Identification

Unique Protocol Identification Number
NCT00409097
Brief Title
Effect of Rosiglitazone on ADMA in Critical Illness
Study Type
Interventional

2. Study Status

Record Verification Date
December 2006
Overall Recruitment Status
Unknown status
Study Start Date
April 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
December 2007 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Amsterdam UMC, location VUmc

4. Oversight

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Critical Illness, Multiple Organ Failure
Keywords
ADMA, MOF, Critical illness

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Rosiglitazone
Primary Outcome Measure Information:
Title
ADMA concentration
Secondary Outcome Measure Information:
Title
SOFA score
Title
Organ function
Title
Mortality

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Milan C Richir, MD
Phone
0031 20 4443601
Email
m.richir@vumc.nl
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Paul am Leeuwen van, MD, PhD
Organizational Affiliation
Amsterdam UMC, location VUmc
Official's Role
Study Director
Facility Information:
Facility Name
VU University Medical Center
City
Amsterdam
ZIP/Postal Code
1081 HV
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Milan C Richir, MD
Phone
0031 20 4443601
Email
m.richir@vumc.nl
First Name & Middle Initial & Last Name & Degree
Milan C Richir, MD

12. IPD Sharing Statement

Learn more about this trial

Effect of Rosiglitazone on ADMA in Critical Illness

We'll reach out to this number within 24 hrs