NCT00660933View on ClinicalTrials.gov

Intravenous Iron Versus Oral Iron for Severe Postpartum Anemia

PHASE4CompletedINTERVENTIONAL
Enrollment

70

Participants

Timeline

Start Date

September 30, 2005

Primary Completion Date

September 30, 2007

Study Completion Date

September 30, 2007

Conditions
AnemiaPuerperal Disorders
Interventions
DRUG

Iron sucrose

Iron sucrose 200 mg/day iv, (20 mg/ml) + 200 cc de NaCl 0,9%/day in 60 minutes per 2 days.

DRUG

NaCl

NaCl 0,9% 200 ml /day iv in 60 minutes per 2 days

Trial Locations (1)

08036

Hospital Clínic of Barcelona, Barcelona

All Listed Sponsors
lead

Hospital Clinic of Barcelona

OTHER

NCT00660933 - Intravenous Iron Versus Oral Iron for Severe Postpartum Anemia | Biotech Hunter | Biotech Hunter