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.
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
- Conditions the study is for
- Febrile Illness Acute, Meningitis, Bacterial, Urinary Tract Infection (Diagnosis)
- 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.
11 sites in 1 country
Sweden11 sites, 11 recruiting
- Recruiting
Sahlgrenska University Hospital
Gothenburg
Pia Laurin, Senior Consultant
Pia Laurin, Senior Consultant
- Not yet recruiting
Helsingborg Hospital
Helsingborg
Kevin Pearsson,, MD, PhD
Kevin Pearsson, MD, PhD
- 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
- Not yet recruiting
Sachs' Children and Youth Hospital
Stockholm
Tobias Alfvén, Professor, MD, PhD
Tobias Alfvén, Professor, MD, PhD
- 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
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
- Age ≤60 days.
- 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.
- Conditions
- Febrile Illness Acute, Meningitis, Bacterial, Urinary Tract Infection (Diagnosis), Invasive Bacterial Infection, Serious Bacterial Infection, Bacteremia
- 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 group | Role | What they receive |
|---|---|---|
| Febrile Infants aged ≤60 days | Febrile 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.
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)
The proportion of investigations, antibiotic treatments, and hospitalizations among febrile infants aged ≤60 days who visited the PED.
Measured: Day 1
The prevalence of meningitis, bacteremia, and urinary tract infection among febrile infants aged ≤60 days.
Measured: 10 days of attendance
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.
- First posted21 Aug 2025
- Study start1 Dec 2025
- Primary completion31 Dec 2027 (estimated)
- Study completion30 Sep 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Febrile Illness AcuteStudies 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 2,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Region Skane
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Orfanos Ioannis, Region Skane
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
Study at a glance
From the registry record, last updated by the sponsor on 2 Apr 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Febrile Infants Swedish Study
- ClinicalTrials.gov ID
- NCT07134751
- Acronym / sponsor ID
- FISS / Dnr 2024-05132-02
- Conditions
- Febrile Illness Acute, Meningitis, Bacterial, Urinary Tract Infection (Diagnosis), Invasive Bacterial Infection, Serious Bacterial Infection, Bacteremia
- Keywords
- Guidelines, Febrile infants, Age ≤60 days, Management, Serious Bacterial Infections, Invansive Bacterial Infections, Clinical prediction tool
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 2,000 participants (estimated)
- Lead sponsor
- Region SkaneUniversity, hospital or other
- Study start
- 1 Dec 2025 (actual)
- Primary completion
- 31 Dec 2027 (estimated)
- Study completion
- 30 Sep 2028 (estimated)
- First posted
- 21 Aug 2025 (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.
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
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
- Age ≤60 days.
- 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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Febrile Infants aged ≤60 days | – | –Febrile Infants aged ≤60 days who present to the pediatric emergency department |
Who may qualify
- Ages
- Up to 60 days
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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.
Key inclusion criteria (2 listed)
- Temperature ≥38.0 C (measured either at home or at the pediatric emergency department)
- Age ≤60 days
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
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
3 secondary outcomes
The proportion of investigations, antibiotic treatments, and hospitalizations among febrile infants aged ≤60 days who visited the PED.
Time frame: Day 1
The prevalence of meningitis, bacteremia, and urinary tract infection among febrile infants aged ≤60 days.
Time frame: 10 days of attendance
Duration and height of the fever, gestational age, birth weight, breastfeeding, clinical signs and symptoms, and laboratory results.
Time frame: Day 1
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 2 Apr 2026.
- Individual participant dataSharing planned: Yes. Anonymised datasets not containing any personal data will be available after publication upon request
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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.
11 sites in 1 country: see every site and its status.
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.