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.
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
- Type of treatment
- Pill or oral medicine, Injection or infusion
- 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.
18 sites in 1 country
Denmark18 sites, 18 recruiting
- 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
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%.
- Conditions
- Bloodstream Infection, Bacteremia Sepsis
- 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 group | Role | What they receive |
|---|---|---|
| Early Oral Switch | Experimental | Early Oral Switch Receives: Drug: Oral antibiotic therapy |
| Standard Intravenous Therapy | Active comparator | Standard 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.
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)
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.
- First posted28 Aug 2026
- Study start1 Sep 2026
- Primary completion1 Nov 2029 (estimated)
- Study completion1 Nov 2029 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Bloodstream InfectionStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Ulrikka Nygaard
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Ulrikka Nygaard, Copenhagen University Hospital, Rigshospitalet
- Investigators
- Ulrikka Nygaard, MD, PhD, DMSc, Principal investigator, Copenhagen University Hospital, Rigshospitalet
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
Study at a glance
From the registry record, last updated by the sponsor on 19 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Early Oral Switch Versus Intravenous Antibiotics in Previously Healthy Children and Adolescents With Bloodstream Infections
- ClinicalTrials.gov ID
- NCT07791914
- Acronym / sponsor ID
- Oral_Switch / H-25090709
- Conditions
- Bloodstream Infection, Bacteremia Sepsis
- Keywords
- Bloodstream Infection, Bacteremia, Pediatric, Children, Oral switch, CHILD, IV-to-oral switch, Antibiotics
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 150 participants (estimated)
- Lead sponsor
- Ulrikka NygaardUniversity, hospital or other
- Study start
- 1 Sep 2026 (actual)
- Primary completion
- 1 Nov 2029 (estimated)
- Study completion
- 1 Nov 2029 (estimated)
- First posted
- 28 Aug 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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%.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Early Oral Switch | Experimental | Drug: Oral antibiotic therapyEarly Oral Switch |
| Standard Intravenous Therapy | Active comparator | Drug: Standard IV antibiotic therapyStandard Intravenous Therapy |
Who may qualify
- Ages
- 4 weeks to 17 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (8 listed)
- 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)
Key exclusion criteria (5 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Oral antibiotic therapyParticipants 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. | Drug | Early Oral Switch |
| Standard IV antibiotic therapyParticipants 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. | Drug | Standard Intravenous Therapy |
Primary outcome
Number of Participants with Treatment Failure
Time frame: Within 8 weeks of randomization
Treatment failure, defined as clinically and/or microbiologically confirmed disease progression or relapse, adjudicated by an independent, blinded adjudication committee.
1 secondary outcome
Intravenous Antibiotic Treatment Duration
Time frame: Within 8 weeks of randomization
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 Oct 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Ulrikka Nygaard, MD, PhD, DMSc principal investigator
Copenhagen University Hospital, Rigshospitalet
18 sites in 1 country: see every site and its status.
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.