Clinical Trials Directory

Trials / Completed

CompletedNCT01895205

Treatment of Women After Severe Postpartum Haemorrhage

A Randomized Comparative, Open-Label Study of Intravenous Iron Isomaltoside 1000 (Monofer®) Administered by High Single Dose In-fusions or Red Blood Cell Transfusion in Women With Severe Postpartum Iron Deficiency Anaemia

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
13 (actual)
Sponsor
Pharmacosmos A/S · Industry
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary purpose of this study is to get explorative information about IV high single dose infusion of iron isomaltoside 1000 compared to RBC transfusion in the treatment of severe PP-IDA evaluated as physical fatigue

Conditions

Interventions

TypeNameDescription
DRUGIron isomaltoside 1000
DRUGRed blood cell transfusion

Timeline

Start date
2013-06-01
Primary completion
2015-08-01
Completion
2015-08-01
First posted
2013-07-10
Last updated
2015-08-19

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT01895205. Inclusion in this directory is not an endorsement.