Completed

Establishment of the Breast Milk Database in China

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What is being collected

Data Collection

No DNA Sample
Who is being recruted

Behavior+1

+ Breast Feeding

+ Feeding Behavior

From 25 to 35 Years
+17 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: October 2016
See protocol details

Summary

Principal SponsorHeilongjiang Feihe Dairy Co. Ltd.
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: October 19, 2016

Actual date on which the first participant was enrolled.

The study cities are Guangzhou, Weihai, Chengdu, Beijing, Harbin, Wuhan, Jinhua, Zhengzhou and Lanzhou. Breast milk will be collected at 9:00-11:00 in the morning from 15 to180 days after giving birth. The nutrients (protein, triglyceride, phospholipid, oligosaccharides and probiotics) in the collected breast milk samples will be measured. These data will be used to establish the breast milk database in China. This databased will provide references for infant nutrient intake and for the formulation and revision of infant formula standards. It will also provide references for the development of new infant formula products in China.

Official TitleEstablishment of the Breast Milk Database in China
NCT03675204
Principal SponsorHeilongjiang Feihe Dairy Co. Ltd.
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

1800 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Female

Biological sex of participants that are eligible to enroll.

From 25 to 35 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

BehaviorBreast FeedingFeeding BehaviorBreast Milk Expression

Criteria

7 inclusion criteria required to participate
Lactating mother 25 ~ 35 years old;

Breast-feeding infants (15 ~180 days old );

Physically healthy by self-evaluation;

Does not smoke;

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10 exclusion criteria prevent from participating
Being treated for gastrointestinal symptoms;

Suffering from mastitis;

Suffering from infectious diseases (tuberculosis, viral hepatitis and HIV infection);

Suffering from cardiovascular disease;

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
This study has no location dataSave this study to your profile to know when the location data is available.
CompletedNo study centers