drugset / Trial / NCT01895218

Treatment of Women After Postpartum Haemorrhage

NCT01895218

Phase 3 Completed 200 enrolled Pharmacosmos A/S BioStata · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary purpose of this study is to compare the efficacy of IV high single dose infusion of iron isomaltoside 1000 to standard medical care in women with PPH evaluated as physical fatigue.

Timeline

Start
2013-06
Primary completion
2014-12
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Iron isomaltoside 1000 Unknown 1200 mg Intravenous

Indications

No indication recorded.