NCT00593619View on ClinicalTrials.gov

Trial Comparing the Safety of Two Different Intravenous Iron Formulations

PHASE4SuspendedINTERVENTIONAL
Enrollment

200

Participants

Timeline

Start Date

January 31, 2008

Primary Completion Date

December 31, 2009

Study Completion Date

December 31, 2009

Conditions
Iron Deficiency AnemiaPerioperative Blood Conservation
Interventions
DRUG

Iron dextran

300mg in 250cc normal saline given over 2 hours

DRUG

Iron sucrose

300mg in 250cc normal saline given over 2 hours

Trial Locations (1)

N6A 5W9

London Health Sciences Centre, London

Sponsors
All Listed Sponsors
lead

London Health Sciences Centre

OTHER