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Mother-infant Microbiota Transmission and Its Link to the Health of the Baby

The Chinese University of Hong Kong logo

The Chinese University of Hong Kong

Status

Enrolling

Conditions

Gut Microbiome
Mother to Child Transmission

Study type

Observational

Funder types

Other

Identifiers

NCT04117321
MOMmy study

Details and patient eligibility

About

The human intestinal tract harbors a diverse and complex microbial community, known as gut microbiota, which is critical in sustaining physiology, metabolism, nutrition and immune function. Dysbiosis of gut microbiota has been linked with obesity, hyperglycemia, hyperlipidemia, inflammatory bowel disease and other chronic inflammatory diseases. Gut microbiota is affected by host genetic markup, diet and life style; and therefore varied by human races and geographical locations.

The development of gut microbiota starts before birth. The infant's microbiome can impact on human health in later life. The microbiome of pregnant women are associated with early-life microbiota of their offspring as well as growth, neurodevelopment and the development of allergic and neurocognitive disorders.

Early childhood, when the microbiota is less mature and more malleable, is a golden age for microbiota manipulation to prevent disease. Studying microbiota at this golden age also allow us to dissect the development of a faulty microbiota and identify therapeutic targets to reverse it and cure diseases that are already developed.

Enrollment

20,000 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Pregnant women

Inclusion Criteria:

  1. Being pregnant
  2. Plan to give birth in local hospital
  3. Competent to provide informed consent (no mental illness or dementia, etc. that will hinder their ability to undertake informed consent)
  4. Plan to stay in the same local area for at least 7 years post-delivery Exclusion Criteria: No

New Born Baby Inclusion Criteria

  1. Be a new born baby of an enrolled pregnant woman
  2. One of the parents or legal guardian is competent to provide informed consent (no mental illness or dementia, etc. that will hinder their ability to undertake informed consent) Exclusion Criteria: No

Father of new born baby Inclusion Criteria

  1. Biological father of an enrolled new born baby
  2. Competent to provide informed consent (no mental illness or dementia, etc. that will hinder their ability to undertake informed consent) Exclusion Criteria: No

Trial design

20,000 participants in 3 patient groups

Pregnant women
Description:
Women who are being pregnant and plan to give birth in local hospital. Pregnant women who plan to stay in the same local area for at least 7 years post-delivery.
New Born Baby
Description:
new born baby of an enrolled pregnant woman.
Father of new born baby
Description:
Biological father of an enrolled new born baby.

Trial contacts and locations

1

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Central trial contact

Jessica Ching; Kitty Cheung

Data sourced from clinicaltrials.gov

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