🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in China / NCT07705685
Active, not recruiting Observational

National Cohort Study on Infant Gut Microbiota and Nutrition

NCT07705685 · tracked via the Priya Life Science China tracker
Sponsor
DiproBio (Shanghai) Co., Ltd.
Phase
Observational
Started
2026-04-30
Last updated
2026-07-15

Condition(s) studied

Fecal Gut Microbiota

Investigational drug(s) / intervention(s)

Fecal sample collection and gut microbiome profiling

Fecal sample collection and gut microbiome profiling: This study is purely observational with no therapeutic or invasive clinical interventions implemented. We only collect non-invasive fecal specimens from enrolled healthy infants and children aged 0-6 years across China, perform microbial genome sequencing and microbial isolation culture to analyze gut microbiota characteristics, and construct a national pediatric gut microbiome atlas. No drugs, medical devices or clinical treatment adjustments are given to participants throughout the research.

Study summary

This study plans to collect 106,667 fecal samples from Chinese infants and children under 6 years old, with multi-dimensional stratification based on geographic location, mode of delivery, antibiotic exposure, and developmental stage. Fecal gut microbiota will be profiled to construct a gut microbiome atlas, establish quantitative analytical models linking geographic regions, physiological phenotypes and microbial signatures, and identify key microbial biomarkers associated with core healthy phenotypes.

Eligibility

Sex
ALL
Min age
0 Years
Max age
6 Years
Healthy volunteers
No
Inclusion Criteria: 1. Infants and children aged 0-6 years, regardless of gender. 2. Volunteers willing to participate in fecal sample collection and baseline health information gathering during the study period. 3. Legal guardians must agree to participate in the study and provide a signed written informed consent. Exclusion Criteria: 1. Presence of congenital developmental anomalies, including but not limited to congenital cardiovascular malformations and chromosomal aneuploidy. 2. Immune system functional disorders, such as Severe Combined Immunodeficiency. 3. Diagnosis of hereditary diseases, such as genetic disorders caused by chromosomal abnormalities. 4. Any condition deemed unsuitable for participation by the investigator, including but not limited to failure to meet compliance assessment standards.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
DiPROBIO(Shanghai) Co., Ltd. Shanghai China
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07705685 on ClinicalTrials.gov ↗ ← All trials in China