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Oral Switch in Bloodstream Infections in Immunocompromised Children (Oral_Switch)

2 novembre 2026 aggiornato da: Ulrikka Nygaard, Copenhagen University Hospital, Rigshospitalet

Oral Switch Versus Standard Intravenous Antibiotics in Children and Adolescents Who Are Immunocompromised and/or a Central Venous Catheter and Uncomplicated Bloodstream Infections: a Nationwide Randomised Controlled Non-inferiority Trial

This nationwide, multicenter, randomized non-inferiority trial aims to determine whether an switch to oral antibiotic therapy (experimental arm) is non-inferior to standard intravenous antibiotic therapy (control arm) with respect to recurrence in children and adolescents with uncomplicated bloodstream infections, who are immunocompromised or have a central venous catheter.

Panoramica dello studio

Descrizione dettagliata

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 therapy or prolonged IV treatment before switching to oral antibiotics. However, these recommendations are primarily based on historical convention and low-quality evidence rather than randomized controlled trials (RCTs). Studies in both adults and children with serious infections other than bloodstream infections suggest that shorter IV courses followed by oral step-down therapy may be safe and effective. However, no RCT has specifically investigated an early switch to oral antibiotic therapy in immunocompromised children and/or those with a central venous catheter (CVC). Although these children may be at increased risk of infectious complications, they also experience a substantial proportion of pediatric bloodstream infections and prolonged IV antibiotic courses. Consequently, the potential impact of a safe early oral-switch strategy may be particularly important in this population.

Objective:

The trial objective is to determine whether early IV-to-oral antibiotic switch is non-inferior to continued standard IV therapy with respect to recurrence of bloodstream infection in clinically stable children and adolescents aged 4 weeks to 17 years with immunosuppression and/or have a CVC and have a bloodstream infection.

Study design:

This is an investigator-initiated, nationwide, open-label, parallel-group, randomized (1:1), controlled, non-inferiority trial, with randomization stratified by 1) Bacteria type (Gram positive vs. Gram negative), and 2) planned CVC removal (removal versus retention or no CVC, as determined before randomization).

Patients:

Children and adolescents aged 4 weeks to 17 years with underlying medical condition associated with immunosuppression and/or the presence of a CVC, and have a 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, and current treatment guidelines. The total antibiotic treatment duration will be the same in both treatment groups, according to Danish guidelines.

Participants will be randomized to the early oral switch arm (experimental arm) or the standard IV arm (control arm).

Participants allocated to the early oral switch arm will receive effective IV antibiotic therapy for at least 3 days and switch to oral therapy as soon as possible after clinical stability, but no later than day 6, to complete a total treatment duration of 10-14 days according to clinical treatment guidelines. Participants allocated to the standard IV arm (control arm) will receive IV antibiotic therapy for the full treatment course.

Sample size calculation:

The study aims to enroll a minimum of 114 participants. The sample size calculation is based on an expected treatment failure risk of 1.5% 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 114 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 114 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 150 participants have been enrolled, whichever occurs first, to increase statistical power to approximately 90%.

Tipo di studio

Interventistico

Iscrizione (Stimato)

114

Fase

  • Fase 4

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

      • Aalborg, Danimarca
        • Department of Pediatrics, Aalborg University Hospital
        • Contatto:
      • Aarhus, Danimarca
        • Aarhus University Hospital
        • Contatto:
      • Copenhagen, Danimarca, 2100
      • Odense, Danimarca
        • Hans Christian Andersen Children's Hospital, Odense University Hospital
        • Contatto:
          • Ulla Hartling, MD PhD
          • Numero di telefono: Ulla.hartling@rsyd.dk

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 4 settimane a 17 anni (Bambino)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  1. Age 4 weeks to 17 years
  2. Underlying medical condition associated with immunosuppression and/or presence of a central venous catheter
  3. Positive blood culture with a high-pathogenic bacterium. Eligible pathogens include Gram-negative bacteria and Gram-positive bacteria such as Staphylococcus aureus, Streptococcus mitis, Streptococcus pneumoniae, β-haemolytic streptococci, and Enterococcus spp., for which standard treatment is at least 7 days of intravenous antibiotics.
  4. Clinical stability, defined as: (a) respiratory and hemodynamically stable, without need for oxygen, IV fluid therapy or inotropic support; and (b) well-appearing with signs of clinical improvement (e.g., improved physical activity), as judged by the investigator
  5. Afebrile for 24 hours.
  6. Tolerating oral fluids and diet and considered to have adequate gastrointestinal absorption for age, as judged by the investigator
  7. Within the randomization window: i) As soon as possible after eligibility is confirmed and ii) within 3-6 days of effective IV antibiotics (72-144 hours) including the duration of the last IV dose.
  8. Informed consent obtained from a parent or guardian, and from the patient if of appropriate age.

Polymicrobial episodes are allowed

Exclusion Criteria:

  1. Complicated infections

    1. Tunnel infection associated with a CVC, unless the CVC is removed
    2. Suspected CNS infection
    3. Other focal infections requiring prolonged antibiotic therapy beyond the treatment of bacteremia, e.g., deep-seated abscess or other deep-seated infections, bone or joint infections, and endocarditis
  2. Blood culture with Pseudomonas aeruginosa, Neisseria meningitidis, or low-pathogenic possible contaminants of uncertain clinical relevance, including coagulase-negative staphylococci, Micrococcus spp., Corynebacterium spp., Cutibacterium acnes, and Bacillus spp.

  3. Clinically significant mucositis (e.g. stomatitis CTCAE (Common Terminology Criteria for Adverse Events) grade ≥3, defined as severe pain interfering with oral intake)

  4. No suitable oral antibiotic available (e.g., due to antimicrobial resistance or contraindications)

  5. Within the follow-up period (≤6 weeks) of a previous randomization for another pathogen covered by the antibiotic indicated for the index episode.

  6. Planned to receive prophylactic antibiotic therapy covering the pathogen after completion of treatment for the index infection

  7. A decision to discontinue life-prolonging treatment has been made, with a life expectancy of less than 6 weeks, as assessed by the treating physician.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Separare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Early Oral Switch

Early Oral Switch

Participants randomized to the experimental arm will switch from IV to oral antibiotic therapy after effective IV antibiotic therapy for at least 3 days, followed by oral therapy as soon as possible after clinical stability, but no later than day 6, and continue oral therapy to complete the recommended total treatment duration.

Comparatore attivo: Standard Intravenous Therapy

Standard Intravenous Therapy

Participants randomised to the control arm will receive IV antibiotic therapy throughout the recommended total treatment duration.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Recurrence of blood stream infection
Lasso di tempo: Within 6 weeks after randomization

Number of patients who experience growth of the same bacteria as in the index blood stream infection in a subsequent blood culture during the follow-up period.

Within 6 weeks after randomization

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
IV antibiotic treatment duration
Lasso di tempo: Within 6 weeks after randomization

Duration of IV antibiotic treatment from randomization until completion of IV antibiotic treatment for the index bloodstream infection, measured in hours.

Within 6 weeks after randomization

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Length of Hospital Stay
Lasso di tempo: From randomization until discharge for the index bloodstream infection, assessed up to 42 days after randomization

Length of Hospital Stay for index infection

From randomization until discharge for the index bloodstream infection, assessed up to 42 days after randomization
Escalation of antibiotics
Lasso di tempo: From randomization until completion of treatment for the index bloodstream infection, assessed up to 42 days after randomization

Proportion of participants with at least one escalation of antibiotic treatment for the index bloodstream infection, defined as a switch from oral to intravenous antibiotics or from intravenous antibiotics to a broader-spectrum intravenous regimen.

From randomization until completion of treatment for the index bloodstream infection, assessed up to 42 days after randomization
Re-initiation of antibiotics
Lasso di tempo: From randomization until completion of treatment for the index bloodstream infection, assessed up to 42 days after randomization

Re-initiation of antibiotics after completion of antibiotic treatment for the index infection (regardless of the indication)

From randomization until completion of treatment for the index bloodstream infection, assessed up to 42 days after randomization
Treatment failure, other than blood stream infection
Lasso di tempo: Within 6 weeks after randomization

Treatment failure, other than blood stream infection, defined as clinically and/or microbiologically confirmed disease progression or relapse, adjudicated by an independent, blinded adjudication committe

Within 6 weeks after randomization
Long term treatment failure
Lasso di tempo: Within 3 months after randomization

Long term treatment failure, including blood stream infection, defined as clinically and/or microbiologically confirmed disease progression or relapse, adjudicated by an independent, blinded adjudication committee

Within 3 months after randomization
Number of Participants with Safety Outcomes
Lasso di tempo: Within 6 weeks after randomization

Safety outcomes are admission to an intensive care unit and death

Within 6 weeks after randomization

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 novembre 2026

Completamento primario (Stimato)

1 novembre 2029

Completamento dello studio (Stimato)

1 febbraio 2030

Date di iscrizione allo studio

Primo inviato

28 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

2 novembre 2026

Primo Inserito (Effettivo)

6 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

2 novembre 2026

Ultimo verificato

1 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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