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Bloodstream InfectionPhase 4Oral_SwitchNCT07791914

Oral Switch in Pediatric Bloodstream Infections

A Phase 4 study testing Oral antibiotic therapy and Standard IV antibiotic therapy in people with Bloodstream Infection and Bacteremia Sepsis, run by Ulrikka Nygaard at 18 sites in Denmark.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This nationwide, multicenter, randomized, non-inferiority trial of children and adolescents with uncomplicated bloodstream infections aims to investigate if early-oral antibiotic switch (experimental arm) is non-inferior to standard intravenous antibiotics (control arm) with respect to treatment failure. Read more about this study

Who is it for?
Ages 4 weeks to 17 years
Conditions the study is for
Bloodstream Infection, Bacteremia Sepsis
What is being tested?
Oral antibiotic therapy and Standard IV antibiotic therapy
Could I receive a placebo?
No, everyone receives an active treatment
How many people
150 participants
Where
18 sitesDenmark
Study dates
1 Sep 2026to 1 Nov 2029
Phase
Phase 4
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 4 weeks to 17 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Age 4 weeks to 17 years
  • Positive blood culture with a i) pathogenic bacterium (eg, Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae, Enterobacterales, Fusobacterium spp. and other pathogenic bacteria) or ii) preliminary blood culture result (eg, Gram-negative rods or Gram-positive cocci in clusters/chains) judged by the investigator to be clinically relevant (ie, not a contaminant) and for which IV antibiotic therapy would be indicated according to standard guidelines
  • Clinical stability, defined as: (a) respiratory and haemodynamic stability, without need for oxygen, IV fluid therapy or inotropic support; and (b) well-appearing with signs of clinical improvement (eg, improved physical activity), as judged by the investigator
  • Tolerating oral fluids and diet, as judged by the investigator
  • Within the randomization window (see below)
  • Informed consent obtained from a parent or guardian, and from the patient if aged 15 years or older
  • Randomization window:
  • Randomization will take place (1) as soon as possible after eligibility is confirmed, and (2) before completion of a maximum of 4 days (96 hours) of effective IV antibiotic therapy, including the duration of the last IV dose (eg, 8 hours for penicillin and 24 hours for ceftriaxone)

Who cannot join

  • Complicated infections: a. Suspicion of endocarditis (echocardiography not performed routinely), b. Suspicion of CNS infection or post-septal cellulitis, c. Foreign material (eg, bone infection involving prosthetic material). d. Complicated postoperative course (eg, perforated appendicitis)
  • Blood culture positive with a. Neisseria meningitidis, b. Streptococcus pneumoniae if afebrile within 24 hours of blood culture collection, c. bacteria considered possible contaminants (eg, coagulase-negative staphylococci, Corynebacterium spp., Micrococcus spp.)
  • Premature infants with a corrected age of less than 28 days
  • No available suitable oral antibiotic (eg, due to antimicrobial resistance or contraindications)
  • Known chronic disease associated with an increased risk of severe infection: i) Immunosuppression, e.g., chemotherapy or biological therapy predisposing to severe infections, ii) Permanent central venous catheter due to an underlying condition, iii) Severe urinary tract abnormalities predisposing to bacteremia, including children receiving prophylactic antibiotic treatment.

Trial locations and contacts

18 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Ulrikka Nygaard, MD, PhD, DMSc contact

+45 40 79 46 56

Ulrikka.Nygaard@regionh.dk

18 sites in 1 country

Denmark18 sites, 18 recruiting
  • Department of Pediatrics, Aabenraa Hospital

    Aabenraa

    Lotte Høeg Hansen, MD, lotte.hoeg.hansen@rsyd.dk

    Recruiting
  • Department of Pediatrics, Aalborg University Hospital

    Aalborg

    Jesper Thaarup, MD, jeth@rn.dk

    Recruiting
  • Aarhus University Hospital

    Aarhus

    Mette Holm, PhD, mette.holm@skejby.rm.dk

    Recruiting
  • Copenhagen University Hospital, Rigshospitalet

    Copenhagen, 2100

    Ulrikka Nygaard, DMSc PhD, Ulrikka.Nygaard@regionh.dk

    Recruiting
  • Department of Pediatrics, Esbjerg Hospital

    Esbjerg

    Anders Egede Sandager Budtz, MD, anders.egede.sandager.budtz@rsyd.dk

    Recruiting
  • Department of Paediatrics and adolescent medicine, NIDO Danmark, Gødstrup Hospital

    Gødstrup

    Luise Borch, PhD, luise.borch@rm.dk

    Recruiting
  • Department of Pediatrics, Herlev Hospital

    Herlev

    Lisbeth Samsoe Schmidt, PhD, lisbeth.samsoe.schmidt@regionh.dk

    Recruiting
  • Department of Pediatrics, Hillerød Hospital

    Hillerød

    Brenda Masomi Kaaya, MD, brenda.masomi.kaaya@regionh.dk

    Recruiting
  • Department of Pediatrics, Hjørring Hospital

    Hjørring

    Pawel Andrej Marcinski, MD, paam@rn.dk

    Recruiting
  • Department of Pediatrics, Holbæk Hospital

    Holbæk

    Dorthe Vestergård Andersen, MD, dva@regionsjaelland.dk

    Recruiting
  • Department of Pediatrics, Hvidovre Hospital

    Hvidovre

    Allan Bybeck Nielsen, PhD, Allan.Bybeck.Nielsen@regionh.dk

    Recruiting
  • Department of Pediatrics, Kolding Hospital

    Kolding

    Kathrine Work Havelund, MD, kathrine.work.havelund@rsyd.dk

    Recruiting
  • Department of Pediatrics, Nykøbing Falster Hospital

    Nykøbing Falster

    Tatjana Zaharov, PhD, tza@regionsjaelland.dk

    Recruiting
  • Hans Christian Andersen Children's Hospital, Odense University Hospital

    Odense

    Ulla Hartling, MD, Ulla.hartling@rsyd.dk

    Recruiting
  • Department of Pediatrics, Randers Hospital

    Randers

    Sabine Frølich Maarbjerg, PhD, sabine.froelich@midt.rm.dk

    Recruiting
  • Department of Pediatrics, Roskilde University Hospital

    Roskilde

    Lise Jensen, MD, lihje@regionsjaelland.dk

    Recruiting
  • Department of Pediatrics, Slagelse Hospital

    Slagelse

    Maren Rytter, PhD, mjry@regionsjaelland.dk

    Recruiting
  • Department of Pediatrics, Viborg Hospital

    Viborg

    Mette Schou Nissen, metnin@rm.dk

    Recruiting

Other trials in Denmark

About this study

Official title: Early Oral Switch Versus Intravenous Antibiotics in Previously Healthy Children and Adolescents With Bloodstream Infections

This nationwide, multicenter, randomized, non-inferiority trial of children and adolescents with uncomplicated bloodstream infections aims to investigate if early-oral antibiotic switch (experimental arm) is non-inferior to standard intravenous antibiotics (control arm) with respect to treatment failure.

Read the detailed description

Background:

Bloodstream infections are among the leading causes of hospital admission and prolonged intravenous (IV) antibiotic therapy in children and adolescents. Current international guidelines recommend IV-only or prolonged IV antibiotic therapy before an oral switch (1,2), but these recommendations rely primarily on historical convention and low-quality evidence rather than randomized controlled trials (RCTs) (1,2). Both adult and pediatric studies suggest that shorter IV courses followed by oral step-down therapy may be safe and effective across a range of serious infections. However, no RCT has explicitly investigated early oral switch in previously healthy children with bloodstream infections.

Objective:

The trial objective is to determine whether early IV-to-oral antibiotic switch, once clinically stable, is non-inferior to continued standard IV therapy with respect to treatment failure in previously healthy children and adolescents aged 4 weeks to 17 years with bloodstream infections.

Study design:

This is an investigator-initiated, nationwide, open-label, parallel-group, randomised (1:1), controlled, non-inferiority trial, with randomization stratified by pathogen group (Staphylococcus aureus, Gram-negative bacteria, and other bacteria).

Patients:

150 previously healthy children and adolescents aged 4 weeks to 17 years with bloodstream infections will be recruited from all 18 pediatric departments in Denmark.

Procedure:

Eligible children will be randomized 1:1 to an early oral switch strategy or standard IV therapy. The choice of oral and IV antibiotics will not be determined by randomization but will be made by the treating clinician according to the isolated pathogen, antimicrobial susceptibility, infectious focus and current treatment guidelines. The total antibiotic treatment duration will be the same in both treatment groups and determined by the site of infection, per Danish guidelines.

Participants allocated to the early oral switch arm (experimental arm) will switch to oral antibiotic therapy as soon as possible after clinical stability and within 4 days after initiation of effective IV antibiotic therapy. Children who have not received antibiotics, or who have received oral antibiotics before the blood culture becomes positive, may also be randomized to oral therapy; thus, prior IV therapy is not required in the experimental arm.

Participants allocated to the standard IV arm (control arm) will continue IV therapy for at least 5 days after initiation of effective IV antibiotic therapy, with 7 days recommended, followed by oral step-down if appropriate.

Sample size calculation:

The study aims to enroll a minimum of 150 participants. The sample size calculation is based on an expected treatment failure risk of 3% in both treatment arms, a non-inferiority margin of 10 percentage points, a one-sided alpha level of 2.5%, and the use of an appropriate statistical method that accounts for the expected low number of events. Assuming a dropout rate of up to 5%, enrollment of 150 participants will provide approximately 80% power to demonstrate non-inferiority.

Recruitment is planned for approximately 36 months and may be extended if required and feasible to achieve the target sample size. If 150 participants are enrolled within the initial 36-month recruitment period, enrollment will continue until the end of the 36-month recruitment period or until a maximum of 200 participants has been enrolled, whichever occurs first, to increase statistical power to approximately 90%.

Being tested
Oral antibiotic therapy, Standard IV antibiotic therapy
Keywords
Bloodstream Infection, Bacteremia, Pediatric, Children, Oral switch, CHILD, IV-to-oral switch, Antibiotics
Medical subject headings
Sepsis, Bacteremia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Oral antibiotic therapyDrug

    Participants randomised to the experimental arm will switch to oral antibiotic therapy as soon as possible after clinical stability and within 4 days after initiation of effective IV antibiotic therapy. Children who have not received antibiotics, or who have received oral antibiotics before the blood culture becomes positive, may also be randomised; thus, prior IV therapy is not required in the experimental arm.

  • Standard IV antibiotic therapyDrug

    Participants allocated to the control group will continue IV therapy for at least 5 days after initiation of effective IV antibiotic therapy, with 7 days recommended, followed by oral step-down if appropriate.

Study groups in NCT07791914
Study groupRoleWhat they receive
Early Oral SwitchExperimentalEarly Oral Switch
Receives: Drug: Oral antibiotic therapy
Standard Intravenous TherapyActive comparatorStandard Intravenous Therapy
Receives: Drug: Standard IV antibiotic therapy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Participants with Treatment Failure

    Treatment failure, defined as clinically and/or microbiologically confirmed disease progression or relapse, adjudicated by an independent, blinded adjudication committee.

    Measured: Within 8 weeks of randomization

Secondary outcomes (1)
  1. Intravenous Antibiotic Treatment Duration

    Duration of intravenous antibiotic treatment from randomization until completion of intravenous antibiotic treatment for the index bloodstream infection.

    Measured: Within 8 weeks of randomization

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Aug 2026
  2. Study start1 Sep 2026
  3. Primary completion1 Nov 2029 (estimated)
  4. Study completion1 Nov 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
150 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07791914
Sponsor's protocol ID
H-25090709
Acronym
Oral_Switch
Status last verified
Aug 2026
First submitted
23 Aug 2026
Last updated
19 Oct 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Oral antibiotic therapy and Standard IV antibiotic therapy in people with Bloodstream Infection and Bacteremia Sepsis, run by Ulrikka Nygaard at 18 sites in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 19 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 18 sites in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Ulrikka Nygaard, MD, PhD, DMSc (+45 40 79 46 56, Ulrikka.Nygaard@regionh.dk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Participants with Treatment Failure (time frame: Within 8 weeks of randomization). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 Oct 2026.

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