drugset / Trial / NCT00396292

Comparison of the Safety and Efficacy of Intravenous Iron Versus Oral Iron in Subjects Who Display Postpartum Anemia

NCT00396292

Phase 3 Completed 361 enrolled American Regent, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This study compares the safety and efficacy of intravenous iron vs oral iron in subjects who display postpartum anemia.

Timeline

Start
2005-02
Primary completion
2005-11
Completion
2006-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ferric carboxymaltose Other / unclassified 1000 mg Intravenous
Comparator Ferrous Sulfate Diagnostic / imaging agent 325 mg Oral

Indications