NL-OMON51243
Not yet recruiting
Phase 4
The efficacy of intermittent versus daily oral iron supplementation in anaemic pregnant women. - FER-IDIP trial (FER Intermittent vs Daily In Pregnancy)
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Anaemia
- Sponsor
- Martini Ziekenhuis
- Enrollment
- 58
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\- Pregnant women of 18 years and older
- •\- Iron deficiency anaemia (defined as: Anaemia (haemoglobin lower than cut\-off
- •value) AND mean corpuscular volume (MCV) 70\-85 fl OR ferritin \<30ug/L) OR mean
- •corpuscular volume (MCV) \< 70fl / hemoglobinopathy is ruled out.
- •\- Adequate mental health
- •\- Good command of the Dutch language
- •\- No participation in other research with medication
- •\- Informed consent
Exclusion Criteria
- •\- Start of iron supplementation at pregnancy duration \> 37 weeks (because of
- •the limited time to achieve an increase in haemoglobin).
- •\- History of bariatric surgery, inflammatory bowel disease, coeliac disease or
- •Helicobacter pylori infection (because of malabsorption of iron).
- •\- Patients who received blood transfusion or parental iron supplementation
- •during the 3 months prior to screening (because of the effect on the
- •haemoglobin level).
- •\- Patients with significant bleeding, blood donation or surgery during
- •pregnancy (because of the effect on the haemoglobin level).
- •\- Allergy for iron.
Outcomes
Primary Outcomes
Not specified
Similar Trials
Unknown
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