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Study on the effect of kestose intake by mother on the gut microbiome of mother and child

A single-blind, randomized, controlled trial of the effect of kestose intake during pregnancy and lactation women on mother and infant microbiome - Fukushima study 2

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs031230592
Enrollment
220
Registered
2024-01-25
Start date
2024-01-25
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Healthy pregnant women and offspring

Interventions

Maternal consumption of 4 g/dose of kestose or maltose twice daily (8 g/day) from 28 weeks of pregnancy until 1 month postpartum.

Sponsors

Nakano Taiji
Lead Sponsor
Shimojo Naoki
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: pregnant woman 1) Pregnant women who are scheduled to continue their prenatal checkups and have their delivery and postpartum checkups at the facility where the study is conducted 2) Pregnant women who are between 20 and 45 years of age at the time of consent 3) Pregnant women who are less than 26 weeks pregnant at the time of consent 4) Pregnant women who have received a full explanation of their participation in this study and who have given written consent of their own free will based on full understanding newborn 1) A newborn whose surrogate has been fully informed of the study, fully understands the study, and has given his/her free and voluntary written consent to participate in the study

Exclusion criteria

Exclusion criteria: pregnant woman 1) Pregnant women with fetal morphological abnormalities, pregnant women with twins or more 2) pregnant women with a history of serious illness 3) Pregnant women who used antibiotics between 20 and 26 weeks of gestation 4) Pregnant women who will be treated with antibiotics at childbirth 5) Pregnant women who are allergic to the test food 6) Pregnant women who will intake of other oligosaccharides or prebiotics during this study period 7) Pregnant women who will participate other study (e.g. other foods, drugs or skin care products) during this study period 8) Pregnant women who cannot understand Japanese 9) Pregnant women who are judged to be ineligible by the principal investigator or subinvestigator newborn 1) Newborns with serious diseases

Design outcomes

Primary

MeasureTime frame
Bifidobacteria counts at 1 month of age in infants born to mothers treated with Kestose and non-treated mothers

Secondary

MeasureTime frame
1) Bifidobacteria count of pregnant women 2) Defecation status (frequency of defecation, fec al characteristics) of pregnant women 3) Total epithelial water loss (TEWL) in infants 4) Specific IgE/TARC level in 6 month old infants 5) Genetic polymorphisms related to skin barrier function (FLG, PNPLA1, SPINK5, and FUT2) in infants

Contacts

Public ContactNaoki Shimojo

Chiba University

shimojo@faculty.chiba-u.jp+81-43-311-3613

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026