ACTRN12609000177257
Completed
未知
A prospective randomised trial to study the effect of intravenous iron therapy versus the standard treatment with oral iron for women diagnosed with iron deficiency anaemia in pregnancy.
aunceston General Hospital0 sites200 target enrollmentApril 17, 2009
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Iron deficiency anaemia in pregnancy
- Sponsor
- aunceston General Hospital
- Enrollment
- 200
- Status
- Completed
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •This trial will be available to all women planning confinement at the Launceston General Hospital (LGH) over a period of 18\-24 months. Pregnant women who are anaemic with Hb level \<116g/L and 18 year old and above are eligible for this study.
Exclusion Criteria
- •Cause of anaemia other than Iron deficiency:Malabsorption syndrome affecting uptake of oral iron Condition associated with iron overload e.g. Haemochromatosis
Outcomes
Primary Outcomes
Not specified
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