Actively Recruiting

Phase Not Applicable
All Genders
NCT06100614

Presepsin to Safely Reduce Antibiotics in Preterm Infants

Led by Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Updated on 2025-10-02

900

Participants Needed

1

Research Sites

118 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In the Netherlands, more than 85% of the preterm infants born \<32 weeks gestational age get antibiotics directly after birth because of the risk of infection with a bacteria. However, only 1 in 70 of these preterm babies actually has a bacterial infection. The use of antibiotics after birth can lead to problems on short term (bowel infection, infection with a bacteria later on or death) or long term (asthma, allergy, obesity). The goal of the PRESAFE trial is to investigate whether addition of a biomarker (presepsin) to the Dutch early-onset neonatal sepsis (EOS) guideline safely reduces unnecessary empirical antibiotic exposure after birth in preterm infants born before 32 weeks gestational age. In this 874-subject multicenter, randomized clinical trial with a concurrent observational cohort, the hypothesis to be tested is that by adding presepsin to the national guideline the amount of unnecessary empirical antibiotic exposure after birth will be reduced with at least 30% without increase in infants with untreated sepsis. The study targets a population of clinical stable very preterm infants with risk factors for eary-onset neonatal sepsis. Antibiotic administration after birth is started to pre-emptively treat EOS. By adding a presepsin-guided step to the Dutch EOS guideline for those infants qualifying for antibiotic treatment, it is assumed that the rate of antibiotic administration can be reduced. However, it is imperative that this reduction in antibiotics is not outweighed by an increase in (culture proven) EOS. Therefore, the co-primary outcomes of the study are: 1) the incidence of culture-proven EOS (non-inferiority) and 2) unnecessary antibiotics prescription i.e. antibiotic administration for ≤ 3 days when started within the first 72 hours after birth (superiority). Secondary outcomes include sepsis-related severity of illness, total number of antibiotic days when started \< 72 hours after birth, and the composite outcome of necrotizing enterocolitis (NEC), late-onset sepsis (LOS), or death until discharge from the initial hospital.

CONDITIONS

Official Title

Presepsin to Safely Reduce Antibiotics in Preterm Infants

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Infants born at a gestational age of 24+0 to 31 6/7 weeks
  • Moderate risk of early-onset neonatal sepsis, meaning infants who should be treated with empirical antibiotics based on the Dutch EOS guideline
Not Eligible

You will not qualify if you...

  • Low risk of early-onset neonatal sepsis with no indication for empirical antibiotics according to the Dutch EOS guideline
  • High risk of early-onset neonatal sepsis defined as:
  • Suspected or confirmed diagnosis of maternal sepsis
  • Suspected or proven EOS in other infants (in case of multiple births) or infants born to mothers with previous infant with GBS disease/infection
  • Unexplained respiratory insufficiency requiring invasive mechanical ventilation and FiO2 >0.40 or non-invasive ventilation with FiO2 >0.60 at time of randomization
  • Ongoing hemodynamic instability requiring inotrope medication or more than one 10 ml/kg fluid bolus at time of randomization
  • Strong clinical concern for sepsis due to physical exam findings such as minimal responsiveness or poor tone

AI-Screening

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Trial Site Locations

Total: 1 location

1

Amsterdam UMC

Amsterdam, North Holland, Netherlands, 1105 AZ

Actively Recruiting

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Research Team

D

Douwe Visser, MD PhD

CONTACT

C

Charlotte Nusman, MD PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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