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Completed

NCT Number: NCT05329701

Individualized Duration of Antibiotic Treatment in Early Onset Infection in Newborns.

A nationwide multicenter open label randomized controlled non-inferiority trial, including 18 departments. The study aims to compare an individualized antibiotic treatment duration with standard seven days of antibiotic treatment for culture negative early-onset infection in term newborns.

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Key information

About this study

There is a documented antibiotic overuse in newborns, and a lack of evidence for the optimal duration of antibiotic therapy in culture-negative infection. The study aims to evaluate the effect of individualized treatment duration in early-onset infection.

The study aims to compare an individualized treatment duration with seven days of treatment for culture negative early-onset infection. The investigators hypothesize that the individualized treatment duration, based on structured clinical assessment of symptoms and level of CRP is non-inferior to the standard care being seven days of treatment. In the experimental treatment arm, antibiotics will be stopped when the participant had 24 hours without symptoms and at same time point have decreasing level of CRP, with an absolute threshold of CRP ≤ 30 mg/l. The investigators hypothesize that individualized treatment will shorten the duration of antibiotic therapy in newborns with early onset infection with very little risk of relapse. Newborns who fulfill criteria to stop antibiotics within 48 hours will not be eligible for inclusion.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Gestational age ≥ 35 weeks
  • Birth weight ≥ 2000
  • Probable or possible infection according to the structured infection risk assessment
  • Sufficient size blood culture, preferably 0.5-1 ml, but at least 0.2 ml, drawn after onset of symptoms but before start of antibiotic treatment
  • Negative blood culture after 48 hours

Exclusion criteria

  • Infants with positive blood culture
  • Blood culture volume prior to antibiotics of < 0.2 ml
  • Site-specific infection as for example, meningitis or osteomyelitis
  • Infant fulfill current recommendation to stop antibiotic treatment at 36-48 hours; Low suspicion of sepsis initially including few and vague symptoms, CRP maximum 35-50 mg/l, negative blood culture and no symptoms after 48 hours of treatment

Treatment and study plan

Individualized treatment duration strategy

Other

As listed under arm description.

Primary outcomes

  1. Readmission due to infection.

    Time frame: From 1-21 days after end of first course of antibiotic treatment.

    Readmission due to infection, defined as symptoms, affected biomarkers and antibiotic treatment > 72 hours

  2. Death

    Time frame: From 1-21 days after end of first course of antibiotic treatment.

    Death of any cause

  3. Total use of antibiotics

    Time frame: From initiation of antibiotics and the next 28 days.

    Use of antibiotics (in hours)

Secondary outcomes

  1. C-reactive protein (CRP)

    Time frame: CRP measured at follow-up 2 days after initial antibiotic treatment ended

    CRP (mg/l) levels at follow-up

  2. Readmission due to infection within 3 months

    Time frame: From 1-100 days after first course of antibiotics ended.

    Readmission due to infection, defined as symptoms, affected biomarkers and antibiotic treatment > 72 hours

Other outcomes

  1. Hospital stay

    Time frame: From initiation of antibiotics and the next 28 days.

    Length of hospital stay within 28 days after initial antibiotic treatment started

  2. Positive blood cultures

    Time frame: From 1-21 days after end of first course of antibiotic treatment.

    Numbers of culture positive infections

  3. Serious adverse events (SAE)

    Time frame: From initiation of antibiotics and the next 100 days.

    Any serious adverse events related to the study intervention

  4. Total use of antibiotics

    Time frame: From initiation of antibiotics and the next 100 days.

    Use of antibiotics (in hours)

  5. Breastfeeding

    Time frame: At 2 day and 21 day follow up, after end of initial antibiotic treatment.

    Exclusive and partial breastfeeding rates

Sponsors and collaborators

Lead sponsor

Ulrikka Nygaard

Other

Collaborators

  • Innovation Fund Denmark
  • University of Copenhagen

Registry information

Official study title

Individualized Duration of Antibiotic Treatment in Culture Negative Early Onset Infection in Term Born Newborns: A Nationwide Randomized Controlled Non-inferiority Trial.

Acronym: DurATi-n

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Apr 15, 2022
Registry last updated
Jan 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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