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
| Type | Name | Description |
|---|---|---|
| DRUG | Iron isomaltoside 1000 | |
| DRUG | Red 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.