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Transfer of Strictly Anaerobe Microbes From Mother to Child (TRAMIC)

M

Medical University of Graz

Status

Completed

Conditions

Microbial Colonization

Study type

Observational

Funder types

Other

Identifiers

NCT04140747
28-524 ex 15/16

Details and patient eligibility

About

This study aims to investigate the changes in the microbiota at different body sites in late pregnancy, in comparison with non-pregnant women, with particular emphasis on archaea, and to identify possible maternal-to-child transfer routes for acquisition of strictly anaerobic microorganisms by analyzing the gut microbiota of new born infants (delivered vaginally or by C-section).

Full description

The investigators hypothesize that changes occur in the microbial community during pregnancy in different body sites (vagina, oral etc.) and that the main source of these microorganisms is the mother for vaginally born infants, while C-section born infants acquire most of the anaerobic microbial communities from other sources rather than mother's vaginal and gut microbiota, such as the environment.

Specific Research Objectives will be:

  1. To investigate diversity of archaea in the vagina of healthy women in the context with community state types (CSTs), and compare vaginal microbiome in pregnant with non-pregnant healthy women.
  2. To identify the presence of archaea in different body sites (oral, gut) or body fluids (amniotic fluid, urine, human milk) within the perinatal microbial communities.
  3. To investigate the presence of archaea in the infant's first-days-of-life intestinal community, and to identify the sources of these microorganisms by using source tracking approach.
  4. To investigate Human Milk Oligosaccharides (HMOs) in maternal (serum, saliva, urine, breast milk) or intrauterine sources (amniotic fluid) as potential modifiers of the microbial communities in these sites.
  5. To analyze associations of maternal/ intrauterine HMOs with infant HMOs and microbiota (meconium and infant stool) in order to investigate vertical transmission of microbiota to the infant.

Enrollment

94 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • healthy women
  • pregnant women: delivery at term (gestational age 37-42); contractions or rupture of membrane no longer than 12h before admission to hospital

Exclusion criteria

  • bacterial/ fungal infections
  • use of antibiotics/ probiotics in past 3 months
  • fetal anomalies
  • multiple pregnancies
  • diabetes type 1, 2, gestational diabetes
  • hypertension, preeclampsia/HELLP
  • HIV ( human immunodeficiency virus), HCV (Hepatitis C)
  • drug abuse, smoking

Trial design

94 participants in 3 patient groups

non-pregnant women
Description:
Samples will be collected from 30 healthy, non-pregnant women in the reproductive age: blood, urine, stool, saliva, oral swabs, vaginal swabs
pregnant women delivering vaginally
Description:
From 30 healthy, pregnant women giving vaginal birth, samples will be collected shortly before, during and after birth from maternal and newborn sites: maternal blood, urine, stool, saliva, oral swabs, vaginal swabs; cord blood, colostrum, meconium, infant oral swabs
pregnant women undergoing C-section
Description:
From 30 healthy, pregnant women giving vaginal birth, samples will be collected shortly before, during and after birth from maternal and newborn sites: maternal blood, urine, stool, saliva, oral swabs, vaginal swabs; amniotic fluid, cord blood, colostrum, meconium, infant oral swabs

Trial contacts and locations

1

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Central trial contact

Evelyn Jantscher-Krenn, PhD; Christine Moissl-Eichinger, PhD

Data sourced from clinicaltrials.gov

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