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Febrile Illness AcuteFISSNCT07134751

Febrile Infants Swedish Study

An observational study of Febrile Illness Acute and Meningitis, Bacterial, run by Region Skane at 11 sites in Sweden.

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

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… Read more about this study

Who is it for?
Ages Up to 60 days
How many people
2,000 participants
Where
11 sitesSweden
Study dates
1 Dec 2025to 30 Sep 2028
Phase
Observational
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 Up to 60 days
  • All sexes
  • No healthy volunteers
  • Child

Study population: All febrile infants aged ≤60 days brought to any of the study Pediatric Emergency Departments will be considered eligible for the study.

Who may be able to join

  • Temperature ≥38.0 C (measured either at home or at the pediatric emergency department)
  • Age ≤60 days

Who cannot join

None listed.

Trial locations and contacts

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

Ioannis Orfanos, Senior Consultant contact

+4646178225

ioannis.orfanos@med.lu.se

11 sites in 1 country

Sweden11 sites, 11 recruiting
  • Sahlgrenska University Hospital

    Gothenburg

    Pia Laurin, Senior Consultant

    Pia Laurin, Senior Consultant

    Recruiting
  • Helsingborg Hospital

    Helsingborg

    Kevin Pearsson,, MD, PhD

    Kevin Pearsson, MD, PhD

    Not yet recruiting
  • Ryhov County Hospital

    Jönköping

    Johan Gyllensvärd, Senior Consultant

    Johan Gyllensvärd, Senior Consultant

    Recruiting
  • Kristianstad Central Hospital

    Kristianstad

    Daniel Gedeborg, Senior Consultant

    Daniel Gedeborg, Senior Consultant

    Recruiting
  • Skåne University Hospital

    Lund

    Ioannis Orfanos, Senior Consultant, PhD

    Ioannis Orfanos, Senior Consultant, PhD

    Recruiting
  • Skåne University Hospital

    Malmö

    Jorge Sotoca Fernandez, Senior Consultant, PhD

    Jorge Sotoca Fernandez, Senior Consultant PhD

    Recruiting
  • Örebro University Hospital

    Örebro

    Andreas Ohlin, Associate Professor, MD, PhD

    Andreas Ohlin, Associate Professor, MD, PhD

    Recruiting
  • Karolinska University Hospital

    Stockholm

    Albano de Juan Plaza, Senior Consultant

    Albano de Juan Plaza, Senior Consultant

    Recruiting
  • Sachs' Children and Youth Hospital

    Stockholm

    Tobias Alfvén, Professor, MD, PhD

    Tobias Alfvén, Professor, MD, PhD

    Not yet recruiting
  • Uppsala University Hospital

    Uppsala

    Susanne Sütterlin, Senior Consultant, PhD

    Susanne Sütterlin, Senior Consultant, PhD

    Recruiting
  • Ystad Hospital

    Ystad

    Madeleine Touma, MD

    Madeleine Touma, MD

    Recruiting

Other trials in Sweden

About this 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

Read the detailed description

BACKGROUND

Each year, around one million febrile infants aged ≤60 days present to pediatric emergency departments (PEDs) in Europe and the United States. Previous studies report that 2-5% of these infants are diagnosed with meningitis or bacteremia (invasive bacterial infections - IBIs) and 10-15% with urinary tract infections (UTIs). Due to the potential severity of these infections, current guidelines recommend comprehensive diagnostic evaluations, hospitalization, and empirical treatment with broad-spectrum antibiotics. Consequently, an estimated 800,000 infants undergo these interventions annually without confirmed SBI.

These practices may have unintended consequences. Lumbar punctures can be painful, stressful, and time-consuming, with unsuccessful attempts linked to longer hospital stays. Early antibiotic exposure has been associated with increased risks of chronic conditions and reduced vaccine response and contributes to antimicrobial resistance. Hospitalization may lead to complications, disrupt breastfeeding, and impose financial and emotional burdens on families. Routine testing can result in overdiagnosis and medical overuse. Additionally, healthcare delivery has environmental implications, with each hospital bed-day generating significant waste and energy consumption.

Current guidelines rely on binary thresholds for biomarkers such as CRP and procalcitonin. They also lack consideration of clinical context, such as the infant's condition or fever characteristics, resulting in a uniform approach that may not suit individual cases.

There is a need for more individualized, evidence-based guidelines that integrate clinical and laboratory findings to support risk stratification and informed decision-making. Guidelines that reduce unnecessary interventions may improve care, optimize resource use, and lessen environmental impact.

The Febrile Infants Swedish Study (FISS) aims to evaluate a new clinical guideline.

PRIMARY AIM

To evaluate the new guideline for the management of infants aged ≤60 days and compare to current praxis.

SECONDARY AIMS

  • To collect clinical data (height/duration of fever, gestational age, birth weight, clinical symptoms/signs, laboratory results, diagnoses) which will enable the improvement of the guideline and the development of a more individualized management guideline.
  • To describe adherence to the new guideline and variation between the study sites in the management of febrile infants aged ≤60 days.

STUDY DESIGN

This will be a multicenter prospective observational study in 11 PEDs in Sweden. All febrile infants presented to the study PEDs will be considered as eligible for the study. The new guideline will be implemented as the PEDs standard management protocol for infants aged ≤60 days with FWS in 7 PEDs (Lund, Malmö, Helsingborg, Kristianstad, Ystad, Örebro, Sachsska-Stockholm). In 4 PEDs (Uppsala, Gothenburg, Jönköping, and Karolinska-Stockholm), the management of febrile infants aged ≤60 days will continue according to current praxis and these PEDs will participate in this study as a control group

STUDY POPULATION

All febrile infants aged ≤60 days brought to any of the study PEDs will be considered eligible for the study.

INCLUSION CRITERIA

  1. Age ≤60 days.
  2. Temperature ≥38.0 C measured either at home or at the PED.

DEFINITIONS

Fever Without a Source (FWS): Defined as a body temperature ≥38°C, measured either at home or in the pediatric emergency department (PED), without an identifiable focus of infection following medical history and physical examination.

Serious bacterial infection (SBI) is defined as a Urinary Tract Infection (UTI), bacteremia, or bacterial meningitis.

Urinary tract infection (UTI) is defined as urine dipstick positive for leukocyte esterase or nitrite and a urine culture with growth of (1) any amount of a single pathogen in samples obtained by suprapubic aspiration; (2) ≥10,000 colony- forming units (cfu)/ml of a single pathogen in samples obtained by a 'clean catch' method or catheterization.

Bacteremia is defined as growth of a bacterial pathogen in a blood culture. The presence of coagulase- negative staphylococci, Propionibacterium spp, Bacillus cereus spp, micrococci, alpha haemolytic streptococci and diphtheroids were considered contaminants, unless indicated otherwise because of clinical or laboratory parameters.

Bacterial meningitis is defined by the presence of a cerebrospinal fluid (CSF) culture or a CSF polymerase chain reaction (PCR) test positive for a bacterial pathogen. Cases with indirect clinical or laboratory indications of bacterial meningitis, such as elevated CSF cell count with positive blood culture and negative CSF culture/PCR, especially if antibiotics are given before the lumbar puncture, can be considered as bacterial meningitis,

Invasive bacterial infection (IBI) is defined as bacterial meningitis or bacteremia.

Delayed treated SBI will be regarded in infants with an SBI who did not receive broad-spectrum antibiotics at the initial management.

Keywords
Guidelines, Febrile infants, Age ≤60 days, Management, Serious Bacterial Infections, Invansive Bacterial Infections, Clinical prediction tool
Medical subject headings
Meningitis, Bacterial, Urinary Tract Infections, Disease, Bacteremia, Sepsis

What participants receive

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

Study groups in NCT07134751
Study groupRoleWhat they receive
Febrile Infants aged ≤60 daysFebrile Infants aged ≤60 days who present to the pediatric emergency department

What is being measured

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

  1. The proportion of febrile infants aged ≤60 days with meningitis, bacteremia, and urinary tract infection identified by the new guideline and the proportion of those that received treatment with delay.

    Measured: 10 days of attendance

Secondary outcomes (3)
  1. The proportion of investigations, antibiotic treatments, and hospitalizations among febrile infants aged ≤60 days who visited the PED.

    Measured: Day 1

  2. The prevalence of meningitis, bacteremia, and urinary tract infection among febrile infants aged ≤60 days.

    Measured: 10 days of attendance

  3. Duration and height of the fever, gestational age, birth weight, breastfeeding, clinical signs and symptoms, and laboratory results.

    Measured: Day 1

Timeline

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

  1. First posted21 Aug 2025
  2. Study start1 Dec 2025
  3. Primary completion31 Dec 2027 (estimated)
  4. Study completion30 Sep 2028 (estimated)

Resources

More details

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

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
2,000 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07134751
Sponsor's protocol ID
Dnr 2024-05132-02
Acronym
FISS
Status last verified
Aug 2025
First submitted
5 Aug 2025
Last updated
2 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Anonymised datasets not containing any personal data will be available after publication upon request

Questions about this trial

What is this clinical trial studying?

An observational study of Febrile Illness Acute and Meningitis, Bacterial, run by Region Skane at 11 sites in Sweden.

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 2 inclusion and 0 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 2 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 11 sites in Sweden. 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.

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 Ioannis Orfanos, Senior Consultant (+4646178225, ioannis.orfanos@med.lu.se), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

The proportion of febrile infants aged ≤60 days with meningitis, bacteremia, and urinary tract infection identified by the new guideline and the proportion of those that received treatment with delay. (time frame: 10 days of attendance). 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 2 Apr 2026; AzTrials last refreshed its copy on 27 Oct 2026.

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