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Analysis of Immunomodulatory Mechanisms and Mining of Bioactive Components in the Human Milk Peptidome Across Different Lactation Stages

Analysis of Immunomodulatory Mechanisms and Mining of Bioactive Components in the Human Milk Peptidome Across Different Lactation Stages

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121998
Enrollment
Unknown
Registered
2026-04-08
Start date
2026-04-20
Completion date
Unknown
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Immune imbalance in infants and young children

Interventions

Colostrum group:None
Transitional milk group:None
Mature milk group:None

Sponsors

Wuxi Maternal and Child Health Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1) Postpartum status: Postpartum time met the grouping requirements of this study, that is, can provide breast milk 0-5 days postpartum (colostrum), 6-15 days postpartum (transitional milk), or 16 days postpartum and more (mature milk). 2) Health status: singleton, full-term (37-42 weeks of gestation) delivery, no major chronic diseases (e.g., diabetes, cardiovascular disease), active infectious diseases (e.g., HIV, viral hepatitis), or autoimmune diseases. 3) Lactation status: voluntary breastfeeding without acute mastitis or other breast diseases that may significantly affect milk composition. 4) Informed consent: fully understand the purpose, process and rights and interests of the study, and voluntarily sign a written informed consent. 3) Lactation Status: Willingness to breastfeed. No acute mastitis or other breast conditions that could significantly affect the composition of breast milk. 4) Informed Consent: Full understanding of the research purpose, procedures, and rights, and voluntary signing of a written informed consent form.

Exclusion criteria

Exclusion criteria: 1) Maternal Illness/Medication: Recent use (e.g., within one week before or after delivery) of medications that may affect the composition of breast milk (e.g., high-dose hormones, immunosuppressants, etc.). 2) Infant Condition: The infant is diagnosed with a major congenital disease, an inherited metabolic disorder, or requires long-term treatment in the neonatal intensive care unit (NICU). 3) Other Factors: Any other conditions judged by the researcher that might affect the representativeness of the samples or increase the risk associated with the study.

Design outcomes

Primary

MeasureTime frame
Proteomics/Peptidomics;

Secondary

MeasureTime frame
Biological pathways enriched by differential peptides;

Countries

China

Contacts

Public ContactRenqiang Yu

Wuxi Maternal and Child Health Hospital

yurenqiang553@163.com+86 150 5067 6990

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026