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Effects of OPO structural lipids and probiotics on infant growth and intestinal health

Effects of OPO structural lipids and probiotics on infant growth and intestinal health

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039422
Enrollment
Unknown
Registered
2020-10-27
Start date
2015-08-01
Completion date
Unknown
Last updated
2021-02-01

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

Conditions

Intestinal flora of healthy infants

Interventions

Group with breastfeeding:Breastfeeding
Group of formula feeding with OPO structure lipids and probiotics:Feeding with formula with OPO structure lipids and probiotics
Group of formula feeding without OPO structure lipids and probiotics:Feeding with formula without OPO structure lipids and probiotics

Sponsors

Zhejiang University School of Medicine Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 0.3 Years

Inclusion criteria

Inclusion criteria: (1) Healthy full-term infants (gestational aged >= 37 weeks, < 42 weeks) with a birth weight of 2.5~4kg were born 1 month after birth. (2) infants who have been exclusively breastfed or formula-fed within the past 72 hours; (3) no congenital abnormalities/birth defects, no genetic metabolic diseases or chromosomal diseases; (4) no family history of metabolic diseases; (5) no history of infectious diseases; (6) the infant's legal guardian agrees to participate in this clinical trial and signs a written informed consent.

Exclusion criteria

Exclusion criteria: (1) Infants with known history of severe allergies of both parents or one parent; (2) patients with diseases or high-risk factors that affect the growth and development of infants, such as 5-minute Apgar score 2 weeks during the neonatal period; (3) complicated with other heart and lung, digestive, nervous, kidney, blood system and other serious primary diseases or birth defects; (4) participated in other clinical trials within 1 month. (5) the investigator considers it inappropriate to participate in the clinical trial.

Design outcomes

Secondary

MeasureTime frame
length;weight;

Countries

China

Contacts

Public ContactShao Jie

Zhejiang University School of Medicine Children's Hospital

shaojie@zju.edu.cn+86 13757181581

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026