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Circulating Markers in Preterm Infants With Perinatal and Neonatal Inflammation (NEOINFLAM)

P

Per Torp Sangild

Status

Terminated

Conditions

Chorioamnionitis
Necrotizing Enterocolitis
Feeding Intolerance
Sepsis

Study type

Observational

Funder types

Other

Identifiers

NCT03320785
NEOINFLAM 2017

Details and patient eligibility

About

Circulating markers to diagnose complications (sepsis, necrotizing enterocolitis) in preterm infants are often inaccurate, partly due to the lack of comprehensive studies with temporal evaluation from birth until a disease onset. The investigators plan to collect weekly blood samples of preterm infants from birth until 4 weeks of age to comprehensively characterize differential protein and epigenetic markers in infants with and without complications (sepsis, necrotizing enterocolitis, chorioamnionitis).

Full description

Preterm infants (10% incidence worldwide), especially those who do not receive sufficient mother's own milk, are susceptible to infectious diseases including sepsis and necrotizing enterocolitis. Infants with history of prenatal inflammation including chorioamnionitis may be at higher risks of acquiring these infectious diseases. Limited knowledge is available regarding a comprehensive temporal profile of circulating markers in preterm infants from birth to disease onset. This current study aims to provide a comprehensive temporal profile of circulating markers, via -omic techniques (proteomics and/or epigenetics), during the first 4 weeks of life in preterm infants with various systemic complications. Thus, this will elucidate a profile of early markers consistently associated with pathological conditions in the whole study period. Depending on the outcome, a subsequent study for validation may be performed.

Primary objective: To characterize circulating markers associated with the early life complications including chorioamnionitis, LOS and NEC in preterm infants during the first four weeks of life.

Secondary objective: To characterize how different feeding regimes and diets may affect these markers during the first four weeks of life in preterm infants

Enrollment

50 patients

Sex

All

Ages

1 to 1 day old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Preterm infants born before the complete 32 weeks of gestation
  • Signed parental consent

Exclusion criteria

  • Major congenital anomalies or birth defects

Trial design

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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