Clinical Trials Directory

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

TypeNameDescription
DRUGFerinject
DRUGFerrous fumarate
DRUGPlacebo for ferrous fumarate
DRUGPlacebo 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.