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Randomized Controlled Trial Of Multiple Micronutrient Versus Iron and Folic acid supplementations on Pregnancy Outcomes in Federal Teaching Hospital , Katsina

Randomized Controlled Trial Of Multiple Micronutrient Versus Iron and Folic acid supplementations on Pregnancy Outcomes in Federal Teaching Hospital , Katsina

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202502706260094
Enrollment
120
Registered
2025-02-03
Start date
2025-03-03
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Feto-maternal care

Interventions

185mg ferrous Fumarate and 400mcg folic acid

Sponsors

self
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: i. Women between gestational ages of 13 to 20 weeks that consent for the study. ii. Women of reproductive age group (15 to 49 years). iii Women who are willing to deliver in our facility.

Exclusion criteria

Exclusion criteria: I. Pregnant women with anaemia in pregnancy II. Pregnant women with G.A <13weeks and above 20weeks G.A. III. Patients that have commenced the use of any of the tested supplements at any time before presentation to the booking clinic in the index pregnancy. IV. Patients with severe, acute or chronic, hepatic or renal failure, cardiac insufficiency. V. Sickle cell disease patients VI. Patients with multiple gestation VII. Non-consenting women VIII. Patient with previous preeclampsia IX. Patient with previous preterm delivery X. Patient with previous postpartum hemorrhage secondary to uterine atony

Design outcomes

Primary

MeasureTime frame
Anemia in the mother and birth weight at delivery in the baby.

Secondary

MeasureTime frame
1 Duration of pregnancy 2 Maternal weight gain at 28weeks and at delivery 3. Neonatal birth weight, length and head circumference, APGAR scores 4. Need for NICU admission 5. Haemoglobin level of pregnant women at 28 weeks and at delivery 6. Detection of pre eclampsia 7. Estimated blood loss at delivery 8. Compliance with supplements 9. Side effects of supplements: 10. Maternal and neonatal outcome such as: 10.1. Abruptio placenta 10.2. Type of delivery 10.3. Miscarriage /still born/neonatal death in the first 24 hours 11. Delivery complications such as: 11.1. Postpartum hemorrhage 11.2. Need for blood transfusion

Countries

Nigeria

Contacts

Public ContactHabib Ibrahim

consultant

ibrahim.habib96@yahoo.com08034418363

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Sep 19, 2026