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Clinical Trial Summary

The primary objective of this study is to compare the total costs to sites and payers of administering IV iron over the 30-day observation period for subjects with IDA who receive Ferric Carboxymaltose (FCM) relative to those who receive iron sucrose, iron dextran, and ferumoxytol.


Clinical Trial Description

The primary objective of this study is to compare the total costs to sites and payers of administering IV iron over the 30-day observation period for subjects with IDA who receive Ferric Carboxymaltose (FCM) relative to those who receive iron sucrose, iron dextran, and ferumoxytol. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01984554
Study type Observational
Source Luitpold Pharmaceuticals
Contact
Status Completed
Phase N/A
Start date September 2013
Completion date December 2014

See also
  Status Clinical Trial Phase
Completed NCT01129843 - Directly Observed Iron Supplementation to Treat Anemia N/A
Completed NCT03754998 - Community Interventions to Improve Iron and Iodine Status in Mother and Child Dyads in Northern Ghana N/A
Completed NCT02410213 - A Study to Characterize the PK and PD Profile of IV FCM in Pediatric Subjects 1-17 Years Old With IDA Phase 2
Active, not recruiting NCT01950247 - Trial to Evaluate the Utility of Serum Hepcidin Levels to Predict Response to Oral or IV Iron and to Compare Safety, Effect on Quality of Life, and Resource Utilization of Injectafer vs Intravenous Standard of Care for the Treatment of IDA in an Infusion Center Setting Phase 4