ISRCTN12911644
Completed
N/A
A pilot clinical trial to test the acceptability and feasibility of different doses of oral iron supplementation to prevent maternal anaemia - PANDA-Dose Study
HS Blood and Transplant0 sites300 target enrollmentApril 27, 2023
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Iron supplementation in pregnant women
- Sponsor
- HS Blood and Transplant
- Enrollment
- 300
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
2024 Results article in https://pubmed.ncbi.nlm.nih.gov/39208353/ (added 02/09/2024)
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Healthy non\-anaemic pregnant women of all parities (haemoglobin concentration (Hb) \> \= 110 g/l) at booking or screening.
- •2\. 13 weeks \+ 6 days gestation or less
- •3\. Age 18 and above
- •4\. Able to give informed consent and willing to fulfil trial requirements
Exclusion Criteria
- •Women with the following conditions will be excluded:
- •1\. Known haemoglobinopathies
- •2\. Anaemia of any type, defined by BSH guidelines
- •3\. Severe gastrointestinal disease, affecting tolerability of oral iron
- •4\. Allergies to iron
- •5\. Multiple pregnancies, given the higher iron demands
- •6\. Known haemochromatosis
- •7\. Recent red cell transfusion, within 1 month
Outcomes
Primary Outcomes
Not specified
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