Trials / Terminated
TerminatedNCT01975272
The Use of Iron Therapy for Patients With Anemia After Caesarean Section
The Value of Iron Treatment for Postoperative Obstetric Patients With Anemia: a Randomized Double Blind Controlled Trial
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 27 (actual)
- Sponsor
- Maastricht University Medical Center · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to determine whether oral or intravenous iron is effective in the treatment of anaemia (iron-poor blood) after caesarean section.
Detailed description
Anemia after caesarean section is often treated with iron therapy to ensure that the hemoglobin will return to normal more rapidly. Scientific evidence for this action is limited. Several studies, in which iron therapy was given after orthopaedic or cardiac surgery, show that after 6 to 10 weeks the hemoglobin was not significantly different between patients treated with oral preparations and patients treated with a placebo. These studies have not examined the hemoglobin level during the first few weeks after surgery including the quality of life analysis. The purpose of this double blind randomized controlled trial therefore is to examine the effect of both oral iron therapy and intravenous iron therapy on hemoglobin level and on the quality of life during the first few weeks postcaesarean in patients with a moderate anemia.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ferinject | |
| DRUG | Ferrous fumarate | |
| DRUG | Placebo for ferrous fumarate | |
| DRUG | Placebo for ferinject |
Timeline
- Start date
- 2015-03-02
- Primary completion
- 2018-05-17
- Completion
- 2018-06-21
- First posted
- 2013-11-04
- Last updated
- 2022-08-22
- Results posted
- 2022-08-22
Locations
2 sites across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT01975272. Inclusion in this directory is not an endorsement.