Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07340450
Eligibility Criteria:
Inclusion Criteria:
1. All women with postpartum anaemia as per operational definition i.e Haemoglobin \<11 g/dl at 24 hours after delivery (either caesarean or SVD).
2. Age 20-40 years.
3. BMI 19-25.
4. Pre-operative haemoglobin \>10 g/dl.
5. Both primiparous and multiparous.
6. Both primigravida and multigravida.
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Exclusion Criteria:
1. Iron Intolerance or previous history of allergy to iron
2. Parenteral Iron hypersensitivity
3. Patients with thalassemia
4. Indication of blood transfusion
5. Patients with bleeding/ clotting disorders
6. Patients with postpartum haemorrhage
7. Patients with chronic diseases.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT07340450
Study Brief:
Protocol Section:
NCT07340450