Atlas of Human Milk Nutrients

N

Nestlé

Status

Completed

Conditions

Breastfeeding Mothers

Study type

Observational

Funder types

Industry

Identifiers

NCT01894893
11.33.NRC

Details and patient eligibility

About

The main objective of this clinical trial is to collect human milk samples from 0 to 4 months after delivery in order to characterize human milk components. The secondary objectives of this study are: To assess whether there is a correlation between human milk composition and mothers' diet To assess whether there is a correlation between human milk composition and maternal clinical parameters To assess whether there is a correlation between human milk composition and mother and infant clinical parameters

Enrollment

370 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Between 18 and 40 years of age included at time of enrolment
  • BMI before pregnancy between 19 and 29 included
  • Having signed the Informed Consent Form
  • Having decided to exclusively breast-feed until infant is 4 months old

Exclusion criteria

  • Currently participating or having participated in another clinical trial during the last 4 weeks prior to the beginning of this study
  • Presenting any disease or medical condition which might prevent breast-feeding or collection the human milk samples or for which breast-feeding is not indicated
  • Presenting diseases/medical conditions such as diabetes, heart problems, abnormal conditions of pregnancy (ex. hypertension)
  • Presenting dietary problems/illnesses such as anorexia, bulimia and celiac disease
  • Assuming any medication indicated for the treatment of any metabolic or cardiovascular disease
  • Cannot be expected to comply with the study procedures

Trial design

370 participants in 1 patient group

Breastfeeding mothers

Trial contacts and locations

13

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems