Comparing Two Intravenous Iron Treatments for Anemia in Kurdish Pregnant Women

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-45
SponsorHawler Medical University

About this trial

The goal of this clinical trial is to compare two types of intravenous (IV) iron-Ferric Carboxymaltose (FCM) and Iron Sucrose (IS)-to learn which one works better to treat iron deficiency anemia in pregnant women who have a clear medical need for IV iron. It will also learn about the safety of both drugs. The main questions it aims to answer are:

1. Does FCM lead to a higher increase in hemoglobin (blood iron) levels 4 weeks after treatment compared to IS? 2. What medical problems or side effects do women experience with each drug? 3. Does FCM reduce the number of hospital visits and improve women satisfaction?

Participants will:

1. Be in their second or third trimester and share the same precise medical indications requiring IV iron (such as severe anemia, no improvement from pills, or being very late in their pregnancy). 2. Be randomly assigned from the start to receive either FCM or IS through an IV, with the total dose calculated based on their body weight and blood tests. 3. Receive FCM in one or more full doses, or receive IS split into multiple smaller sessions up to 3 times a week. 4. Visit the clinic for their assigned infusions and undergo blood tests and satisfaction surveys twice: right before starting treatment and 1 month after receiving the medication.

Eligibility criteria

Qualifiers

Parity: All parity levels accepted (Para 0, Para 1, Para 2-4, and Para 5 or more).

Pregnancy Stage: Currently in the second or third trimester of pregnancy (greater than 14 weeks gestation).

Confirmed Iron Deficiency Anemia (IDA): Documented Hemoglobin (Hb) less than 11 g/dL AND Serum Ferritin less than 30 ng/mL.

Intolerance to oral iron therapy (e.g., severe nausea, severe constipation, or gastrointestinal distress).

Disqualifiers

First trimester of pregnancy (less than or equal to 14 weeks gestation).

Known hypersensitivity, allergy, or previous severe adverse reaction to intravenous iron formulations or any of their components.

Anemia due to causes other than iron deficiency (e.g., vitamin B12 or folate deficiency, hemoglobinopathies, anemia of chronic disease).

Active, severe systemic infection.

Trial design

Treatments tested in this trial

  • Intravenous Ferric Carboxymaltose (FCM)
  • Iron Sucrose (IS) Infusion

Treatment groups

400 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators