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Recruiting NCT05462366

Omics Sequencing of Specimen Derived From Mother-Infant-Pairs

Observational Healthy Breast-milk Collection Feces

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Sample collection.
Who it may be relevant to
Registry conditions: Healthy, Breast-milk Collection, Feces. Basic parameters: up to 40 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The investigators aim to collect breast-milk and feces from the participants, and apply culture techniques as well as omics sequencing technology to probe into the microbial and metabolomic signature of the specimens.

Interventions

  • Other Sample collection
    Collect breast-milk and feces from mother-infant-pairs.

Primary outcome measures

  • Compare the omics differences of the specimens between the experimental and control groups [Time frame: 2021.7.1-2026.12.30]
  • Compare the microbial feature differences of the specimens between the experimental and control groups [Time frame: 2021.7.1-2026.12.30]
Secondary outcome measures (1)
  • Compare the health status differences between the experimental and control groups [Time frame: 2021.7.1-2026.12.30]

Eligibility criteria

Inclusion criteria

  • healthy pregnant women aged between 20y and 40y.
  • Vaginal birth
  • BMI<23.5 before pregnancy
  • Infants' birth weight, between 2500g and 4000g.

Exclusion criteria

  • gestational diabetes
  • diagnosis of depressive disorder during pregnancy
  • gestational hypertension
  • diagnosis of other diseases during pregnancy
  • Under probiotics or antibiotic treatment from 3 months prior to pregnancy till 3 months after delivery
  • histrory of smoking and drinking alcohol
  • history of diarrhea from 3 months prior to pregnancy till 3 months after delivery

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Family-based

Study locations

China · 1 center
  • Zhujiang Hospital — Guangzhou

Identifiers

NCT: NCT05462366 · ZhujiangHFCYXZX

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗