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Completed

NCT Number: NCT01712165

Micronutrient-supplemented Milk Study in Women of Childbearing Age

The purpose of this study is to determine if consuming ANMUM Materna (a fortified milk product) over a 12-week period increases red blood cell folate concentrations in women of childbearing age in Singapore, compared to an equivalent amount of standard (unfortified) milk.

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Key information

Age range

21 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Changi General Hospital

Singapore, 529889

About this study

Folic acid (~400 µg/day) taken around the time of conception significantly reduces the risk of a neural tube defect (NTD)-affected pregnancy. Strategies to reduce NTD with folic acid, include supplement use and food fortification. An attractive strategy for NTD prevention is the use of fortified foods targeted for use by women planning a pregnancy. Fonterra currently markets a fortified-milk (ANMUM Materna) in Asia, designed for use prior to and during pregnancy. This milk product, if consumed as directed, provides ~400 µg folic acid per day. It is not known whether ANMUM Materna will reduce NTD rate. However, in a case-control study the risk of NTD was inversely associated with maternal red blood cell (RBC) folate concentrations. Accordingly, if ANMUM Materna increases RBC folate, it could be expected to decrease NTD risk.

In this study, the ANMUM Materna fortified milk will be tested against a standard control (unfortified) milk over a 12 week period. The subjects will consume 75g of milk powder daily throughout the supplementation period.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Female 21-35 years old.
  • Able to understand the nature and purpose of the study, including potential risks and side effects.
  • Willing to consent to study participation and to comply with study requirements.
  • Negative Pregnancy test at screening

Exclusion criteria

  • Consumption of vitamins and/or mineral supplements known to contain folate 6 months prior.
  • Chronic disease.
  • Milk and/or lactose-intolerant.
  • Pregnancy in the last 12 months, or currently planning a pregnancy.
  • Prior history of NTD-affected pregnancy
  • Serum Folate deficiency

Treatment and study plan

ANMUM Materna

Dietary Supplement

Control (milk powder)

Dietary Supplement

Primary outcomes

  1. Increase in red blood cell folate concentration

    Time frame: 12 weeks

    To determine if consuming ANMUM Materna over a 12-week period increases red blood cell folate concentrations in women of childbearing age in Singapore, compared to an equivalent amount of standard (unfortified) milk.

Secondary outcomes

  1. Reduction in homocysteine concentration

    Time frame: 12 weeks

    To determine if consuming ANMUM Materna over a 12-week period lowers homocysteine concentrations in women of childbearing age, compared to an equivalent amount of standard (unfortified) milk.

  2. Increase in plasma folate concentration

    Time frame: 12 weeks

    To determine if consuming ANMUM Materna over a 12-week period increases plasma folate concentrations in women of childbearing age, compared to an equivalent amount of standard (unfortified) milk.

  3. Increase in plasma vitamin B12 concentration

    Time frame: 12 weeks

    To determine if consuming ANMUM over a 12-week period increases plasma vitamin B12 concentrations in women of childbearing age, compared to an equivalent amount of standard (unfortified) milk.

Sponsors and collaborators

Lead sponsor

Fonterra Research Centre

Industry

Collaborators

  • Changi General Hospital

Registry information

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Oct 23, 2012
Registry last updated
Oct 11, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.