Regulation and Mechanism of New Compound Functional Ingredients in Infants
NCT ID: NCT05297006
Last Updated: 2022-03-25
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
180 participants
OBSERVATIONAL
2022-04-01
2022-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Breastfeeding group
The mother can breastfeed exclusively until the infants is at least 4 months old, after which complementary foods are added scientifically according to the baby's condition.
No interventions assigned to this group
Formula group containing new compound functional ingredients
Only use formula milk powder containing oligosaccharides, sialic acid and other ingredients feed the infants for at least 4 months, and then complementary food is added scientifically according to the infant's condition.
The infants who drank milk powder were given a dietary intervention four months before
The infants who eat milk powder were randomly divided into two groups: group containing new compound functional ingredients and group without new compound functional ingredients
Formula group without new compound functional ingredients
Only use formula milk powder without oligosaccharides, sialic acid and other ingredients feed the infants for at least 4 months, and then complementary food is added scientifically according to the infant's condition.
The infants who drank milk powder were given a dietary intervention four months before
The infants who eat milk powder were randomly divided into two groups: group containing new compound functional ingredients and group without new compound functional ingredients
Interventions
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The infants who drank milk powder were given a dietary intervention four months before
The infants who eat milk powder were randomly divided into two groups: group containing new compound functional ingredients and group without new compound functional ingredients
Eligibility Criteria
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Inclusion Criteria
2. Full-term (gestational age ≥37 weeks);
3. Birth weight 2500-4500g;
4. Mothers have no history of diabetes, hypertension, heart disease, and other diseases during pregnancy;
5. The guardian signed informed consent and voluntarily enrolled into the group and promised to complete systematic follow-up.
Exclusion Criteria
2. History of birth asphyxia (Apgar score \< 3)
3. Severe allergy to milk and serious medical conditions such as intracranial hemorrhage, chronic diarrhea, necrotizing colitis, or acute infection
4. The guardian refused to enroll or could not complete the system follow-up.
ALL
Yes
Sponsors
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Peking University First Hospital
OTHER
Peking University People's Hospital
OTHER
Peking University Third Hospital
OTHER
Responsible Party
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Locations
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Peking University People's Hospital
Beijing, Beijing Municipality, China
Peking University Third Hospital
Beijing, Beijing Municipality, China
Peking University First Hospital
Beijing, , China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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S170003
Identifier Type: -
Identifier Source: org_study_id
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