RecruitingNot ApplicableNCT06425796

Adiposity and Iron Requirements in Pregnancy

Impact of Maternal Adiposity on Maternal Iron Status and Requirements: a Randomised Intervention Study


Sponsor

University of Ulster

Enrollment

312 participants

Start Date

May 20, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to explore how body fat influences the response to either 25 or 50 mg of daily iron supplements during pregnancy. We will conduct a double-blind randomized controlled intervention study involving 312 pregnant women recruited from antenatal clinics in the Northern Trust Area. Participants will be randomly assigned to receive either 25 or 50 mg of iron per day from 12 weeks of pregnancy until delivery, using the Active Iron supplement brand. Blood samples will be collected at 12, 28 and 36 weeks gestation and umbilical cord blood will be collected at delivery. Anthropometric measurements will be taken at each visit, and participants will complete questionnaires on various aspects of health and lifestyle, mental health, gastrointestinal symptoms, and compliance.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Adiposity and Iron Requirements in Pregnancy (ADIPREG) for people with iron deficiency anemia of pregnancy. The study is currently recruiting participants at 3 locations. People eligible for this study include women aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIETARY_SUPPLEMENTAdiposity and Iron Requirements in Pregnancy (ADIPREG)

Iron 25 arm will receive: two iron supplements containing 12.5 mg of elemental iron + 1 multivitamin supplement (they will receive a total of 3 supplements per day). Iron 50 arm will receive: two 25 mg elemental iron supplements + 1 multivitamin supplement (they will receive a total of 3 supplements per day). The multivitamin supplement will contain folic acid, vitamin B1, vitamin B2, vitamin B3, vitamin B5, vitamin B6, vitamin B12, vitamin C and vitamin D. In summary, each participant will receive 3 supplements per day and instructed to take the 3 supplements together, in the morning, with breakfast. Supplements will be given to the participants when they attend for their clinic appointment. The intervention will begin at 12 gestational weeks and continue until the baby is delivered.


Locations(3)

Causeway Hospital

Coleraine, Co Londonderry, United Kingdom

Causeway Hospital

Coleraine, Co. Londonderry, United Kingdom

Ulster University,Human Intervention Studies Unit,

Coleraine, Co. Londonderry, United Kingdom

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NCT06425796


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