Invasive Bacterial Infection

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Review clinical trials related to Invasive Bacterial Infection. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Early Discontinuation of Antibiotics in Paediatric High-risk Febrile Neutropenia

The goal of this clinical trial is to evaluate whether stopping antibiotic treatment early is safe in paediatric patients with cancer who develop high-risk febrile neutropenia but show good clinical evolution and low biomarker levels 48-72 hours after the episode. The main questions it aims to answer are: Is early discontinuation of antibiotics as safe as the standard strategy in terms of preventing invasive bacterial infections (such as sepsis, microbiologically documented infection, ICU admission, or death)? Does this strategy reduce the number of days on antibiotics without increasing infection-related complications? Researchers will compare early antibiotic discontinuation with the standard care strategy to see whether the early-stop approach provides similar safety while reducing antibiotic exposure. Participants will: Receive standard initial antibiotic therapy for febrile neutropenia. Undergo clinical and biomarker evaluations (including CRP and PCT). Be randomly assigned to: Experimental group: early discontinuation of antibiotics, or Control group: continuation of the standard antibiotic strategy. Be followed for 28 days after randomisation to monitor safety outcomes and treatment effects.

Participants needed: 136
Trial details
Phase: Phase 4Age: Up to 18Biological sex: AllType: InterventionalSponsor: Hospital Universitari Vall d'Hebron Research InstituteUpdated: May 15, 2026Locations: 4
Eligibility criteria

Acute myeloblastic leukaemia at any phase of chemotherapy [+20]

Antibiotic treatment at the time of the FN episode different from that used prop... [+6]

Status: Recruiting

Febrile Infants Swedish Study

Approximately one million febrile infants aged ≤60 days present annually to pediatric emergency departments (PEDs) in Europe and the United States. Although fewer than 5% are diagnosed with meningitis or bacteremia (invasive bacterial infections - IBIs), and 10-15% with urinary tract infections (UTIs), current guidelines recommend extensive diagnostic evaluations, hospitalization, and empirical treatment with broad-spectrum parenteral antibiotics. This approach may contribute to medical overuse, with implications for patient care, healthcare resource utilization, and environmental sustainability. The Febrile Infants Swedish Study (FISS) is a prospective observational study conducted across 11 PEDs in Sweden. All febrile infants aged ≤60 days presenting to participating sites will be eligible. A new clinical guideline for the management of infants with fever without source (FWS) will be implemented in 7 PEDs, while 4 PEDs will continue with current standard practice and serve as a comparison group. The study is expected to run for approximately two years and aims to recruit a minimum of 2,500 febrile infants

Participants needed: 2,000
Trial details
Age: Up to 60Biological sex: AllType: ObservationalSponsor: Region SkaneUpdated: Apr 2, 2026Locations: 11
Eligibility criteria

Temperature ≥38.0 C (measured either at home or at the pediatric emergency depar... [+1]

Status: Recruiting

CommunautAry Pediatric bacteRial Infection in Intensive CarE Unit

Severe bacterial infections are a worldwide scourge. However, the epidemiology of this type of infection varies over time. It is therefore essential to monitor them in order to prevent them more effectively. At this time, in France, no monitoring exists for this kind of infections.

Participants needed: 3,000
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: Association Clinique Thérapeutique Infantile du val de MarneUpdated: Mar 19, 2026Locations: 1
Eligibility criteria

Age <18 years (only hospitalized children) [+1]

Refusal by one of the parents or by Child in understanding age [+1]

Status: Not yet recruiting

PATH Study: People With Injecting Related Infections: Assessing Treatment Outcomes for Those Who Are Hospitalised.

We seek to characterise the burden and outcomes of and understand the current experience of people who inject drugs admitted to hospital with invasive injecting-related infections, in order to implement and evaluate strategies to improve completion of therapy and reduce patient-directed discharges, with ultimate benefit to the patient and health service.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Kirby InstituteUpdated: Feb 20, 2024
Eligibility criteria

Have voluntarily signed the informed consent form, [+3]