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OpenTrials
Completed

NCT Number: NCT01805011

Study on Normal Ranges of Lipids in Breast Milk of Healthy Mothers

This trial is undertaken to better understand the ranges of functional components normally found in human milk. This will strengthen the scientific knowledge on breast-milk composition as a "gold standard".

Completed

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Key information

Conditions

Healthy Mothers

Age range

18 year–40 year

Sex eligibility

Female

Study type

Observational

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Gestational age between 37 and not above 42 weeks
  • 18 years old ≤ Mother ≤ 40 years old
  • 18.5 ≤ pre-pregnancy BMI ≤ 29
  • Mothers willing to breastfeed for the first 4 months

Exclusion criteria

  • Gestational diabetes
  • HTA < 140/90
  • Mothers who are smokers while breast-feeding

Treatment and study plan

minimum 4 months of breastfeeding

Other

Primary outcomes

  1. levels of lipids

    Time frame: After 1 month of Breastfeeding

    The primary objective of this trial is to determine the levels of lipids normally found in the breast-milk of healthy lactating mothers

Secondary outcomes

  1. profile and quantity of sugars

    Time frame: After 1 month of breastfeeding

    Secondary objectives include the measure of the profile and quantity of sugars found in human milk

Sponsors and collaborators

Lead sponsor

Société des Produits Nestlé (SPN)

Industry

Registry information

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Mar 5, 2013
Registry last updated
Sep 19, 2024

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.

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