Dexamethasone for Cardiac Surgery Trial

Status Completed

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Cardiac Diseases
Heart Diseases
Postoperative Complications
Systemic Inflammatory Response Syndrome

Clinical Trial Details

NCT number	NCT00293592
Study type	Interventional
Source	UMC Utrecht
Contact
Status	Completed
Phase	N/A
Start date	May 2006
Completion date	December 2012

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