Clinical Trials Directory

Trials / Completed

CompletedNCT02458625

A Comparison Between Intravenous Iron Sucrose to Its Combination With Oral Iron Supplements for the Treatment of Postpartum Anemia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
158 (actual)
Sponsor
HaEmek Medical Center, Israel · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is aimed to compare the efficacy of two mode of iron administration to treat post partum anemia - a single dose of intravenous iron sucrose versus a single dose of iron sucrose and 6 weeks of treatment with oral iron supplement.

Detailed description

Anemia is common following delivery. It is associated with disturbing symptoms such as fatigue, cognitive impairment and syncope in severe cases. International guidelines recommend to use intravenous iron sucrose to treat intermediate and severe anemia until the target hemoglobin is achieved. However, patient's compliance after delivery is low, making the administration of several doses difficult. In those cases oral iron supplements might be used. In the present study the investigators will compare the efficacy of two iron administration protocols to treat post partum anemia - a single dose of intravenous iron sucrose versus a single dose of iron sucrose and 6 weeks of treatment with oral iron supplement.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTIron sucrose 500 mg
DIETARY_SUPPLEMENTIron bisglycinate 60 mg

Timeline

Start date
2016-04-01
Primary completion
2020-06-07
Completion
2020-11-04
First posted
2015-06-01
Last updated
2020-11-06

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT02458625. Inclusion in this directory is not an endorsement.