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Maternal and Neonatal Microbiome

H

Hadassah Medical Center

Status

Withdrawn

Conditions

Microbiota

Treatments

Other: non invasive sampling

Study type

Observational

Funder types

Other

Identifiers

NCT02891746
Mat-Neo-Micro-HMO-CTIL

Details and patient eligibility

About

The aim of the study is to characterize and monitor the microbiome of premature infants born in the investigators facility until discharge from the NICU. The investigators will also examine the relationship between mode of delivery and the microbiome of the infant, while exploring various possible factors that may affect it. In addition, the investigators will compare the microbiome of premature infants to the microbiome of term babies born at the same time in the same facility.

Sex

All

Ages

Under 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Premature infants ≤ 34 weeks of gestation admitted to the Neonatal Intensive Care Unit at Hadassah University Hospital, Mount Scopus and their mothers.

The control group:

  • Neonates ≥ 37 weeks gestation of which 50 were delivered vaginally and 50 by Caesarean section at Hadassah University Hospital, Mount Scopus and their mothers.

Exclusion criteria

  • Neonates with congenital anomalies or metabolic conditions.

Trial design

0 participants in 2 patient groups

Premature infants
Description:
premature infants ≤ 34 weeks of gestation
Treatment:
Other: non invasive sampling
Term infants
Description:
neonates ≥ 37 weeks gestation
Treatment:
Other: non invasive sampling

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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