Triage Performance and Physiological Predictors of Serious Illness in Febrile Children in the Pediatric Emergency Department

NCT07739004 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 3000

Last updated 2026-08-05

No results posted yet for this study

Summary

This multicenter prospective observational cohort study evaluates how well the initial triage category assigned by the Turkish Ministry of Health three-level color-coded triage system (Red-Yellow-Green) predicts serious clinical outcomes in children aged 0-18 years who present with fever to pediatric emergency departments. The study additionally assesses whether physiological parameters recorded at triage (heart rate, respiratory rate, oxygen saturation, capillary refill time, AVPU level of consciousness, and general appearance) provide independent and incremental prognostic value beyond the assigned triage category. Ten centers across Turkey will enroll consecutive eligible febrile children over a 3-month period. Routine clinical care and triage decisions are not altered by the study. The primary outcome is a composite serious clinical outcome. The study is reported in accordance with the STROBE and TRIPOD statements.

Conditions

  • Fever
  • Triage
  • Pediatric Emergency Medicine
  • Serious Bacterial Infection
  • Sepsis

Interventions

DIAGNOSTIC_TEST

Ministry of Health three-level color-coded triage

At presentation, each child is assigned a triage category (Red, Yellow, or Green) by the triage nurse using the Turkish Ministry of Health three-level color-coded system, and physiological parameters (heart rate, respiratory rate, oxygen saturation, capillary refill time, AVPU level of consciousness, and general appearance) are recorded on a standardized triage form. This reflects routine care and is not modified for the study.

Sponsors & Collaborators

  • Kayseri City Hospital

    collaborator OTHER_GOV
  • Adana City Training and Research Hospital

    collaborator OTHER
  • Cukurova University

    collaborator OTHER
  • Akdeniz University

    collaborator OTHER
  • Manisa Celal Bayar University

    collaborator OTHER
  • Eskisehir Osmangazi University

    collaborator OTHER
  • Lütfi Kırdar City Hospital

    collaborator OTHER
  • Dokuz Eylul University

    collaborator OTHER
  • Tokat Gaziosmanpasa University

    collaborator OTHER
  • TC Erciyes University

    lead OTHER

Principal Investigators

  • Yilmaz Secilmis · TC Erciyes University

Eligibility

Min Age
0 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-07-28
Primary Completion
2026-11-01
Completion
2026-12-01

Countries

  • Turkey (Türkiye)

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07739004 on ClinicalTrials.gov