Dexamethasone for Cardiac Surgery Trial

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
D van Dijk, UMC Utrecht
ClinicalTrials.gov Identifier:
NCT00293592
First received: February 16, 2006
Last updated: April 18, 2015
Last verified: April 2015

February 16, 2006
April 18, 2015
May 2006
November 2011   (final data collection date for primary outcome measure)
Composite endpoint of mortality, myocardial infarction, stroke, renal failure and prolonged mechanical ventilation (> 48h) [ Time Frame: 30 days postoperatively ] [ Designated as safety issue: No ]
Not Provided
Complete list of historical versions of study NCT00293592 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Dexamethasone for Cardiac Surgery Trial
Dexamethasone for Cardiac Surgery Trial

This is a multicenter, randomized, double-blind trial, comparing clinical outcomes after the administration of high-dose dexamethasone versus placebo in patients undergoing heart surgery with the use of cardiopulmonary bypass. The primary endpoint is the occurrence of major complications (including all-cause mortality, myocardial infarction, stroke, renal failure, and prolonged mechanical ventilation) in the first 30 days after surgery.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
  • Systemic Inflammatory Response Syndrome
  • Cardiac Diseases
  • Postoperative Complications
Drug: Dexamethasone
1 mg per kg as a single dose before initiation of cardiopulmonary bypass
  • Active Comparator: Dexamethasone
    Intervention: Drug: Dexamethasone
  • Placebo Comparator: Placebo
    Intervention: Drug: Dexamethasone

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
4500
December 2012
November 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • All types of cardiac surgery in which cardiopulmonary bypass is used

Exclusion Criteria:

  • Age under 18 years
  • Life-expectancy < 6 months
  • Emergency operations
  • Re-operations within the same admission
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Netherlands
 
NCT00293592
DECS
Yes
D van Dijk, UMC Utrecht
UMC Utrecht
Not Provided
Study Chair: CJ Kalkman, MD, PhD UMC Utrecht
Study Director: D van Dijk, MD, PhD UMC Utrecht
UMC Utrecht
April 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP