Chelated Oral Iron Versus Intravenous Iron Sucrose for Treatment of Iron Deficiency Anemia Late in Pregnancy

Trial statusAvailable
Trial phaseNot listed
Trial typeExpanded Access
Biological sexFemale
Age18+
SponsorAssiut University

About this trial

compare the efficacy and safety of intravenous iron sucrose versus chelated oral iron in the treatment of iron deficiency anemia late in pregnancy.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Women aged 18 years or more with established iron deficiency anemia ( Hb: 8-10 )

Pregnancy 26-34 weeks

Disqualifiers

Anemia due to other causes than iron deficiency anemia.

Recent blood transfusion (in the last 3 months ).

Allergy to iron.

Multiple pregnancy.

Trial design

Treatments tested in this trial

  • Chelated Iron

    Drug

    Treatment will be started 24rh after initial visit women will be randomized used random sequence computer generated list in such a way that every patient had equal chance to be among any of the two groups either to group 1 , where they will receive I.V ferrous sucrose in the E.U in Women's Health Hospital Assuit University as an i.v infusion in 250 ml 0.9% sodium chloride slowly over 30 minutes. The total required dose of iron will be divided into three doses, which will be given every 3 days, and the maximum daily dose is 200mg ( 2 ampoules ).

  • Iron sucrose

    Drug

    to group 2 where they will receive chelated oral iron, they will be given iron chelated amino acid containing 15 mg of elemental iron once daily for 6 weeks. the women will be advised to take 1 tab of iron chelated amino acid containing 15mg of elemental iron once daily with meals for 6 weeks from the day of recruitment.

Treatment groups

No treatment groups listed

Trial outcomes

This trial has no outcomes listed.

Locations

This trial has no locations.

Sponsors and contacts

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