Management and Outcome of Fever in Children in Europe

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

38480 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-01-01

Study Completion Date

2021-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This is an observational study assessing the management and outcome of children presenting to Emergency Departments (ED) with fever across Europe.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Treatment of Hyperpyrexia and in the Pediatric Emergency Department (FEVER_ED)

NCT06194383

Fever

ACTIVE_NOT_RECRUITING

Prescription Antipyretics to Decrease Unscheduled Return Visits In A Pediatric Emergency Department

NCT07074912

Fever

RECRUITING NA

Outpatient Use of Analgesics in Children and Adolescents in France

NCT03371043

Outpatient Use of Analgesics in Children and Adolescents

COMPLETED

The Effect of Methods Used in Oral Antipyretic Administration on the Vital Findings of the Child With Fever

NCT05366049

Fever Heart Rate Respiratory Rate +1 more

COMPLETED NA

Measuring the Metabolic Cost of Fever

NCT02939781

Child Critical Illness Fever

TERMINATED

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

This is an observational study assessing the management and outcome of children presenting to Emergency Departments (ED) with fever across Europe. This study will use large departmental datasets to collect information on at least 50,000 febrile episodes . This study will use large-scale, pseudo-anonymized departmental data, and will not involve consented patient recruitment; nor will it use patient samples. Data included in MOFICHE will be based on that collected as part of routine clinical care. Antibiotic prescription, hospitalisation and number/type of investigations, re-attendance at ED within 5 days of the first hospital presentation will be recorded.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Antibiotic Prescription

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

antibiotic prescription

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* aged 0- 18 years visiting the emergency care.
* fever measured at ED or history of (measured) fever less than 3 consecutive days prior to presentation at emergency department