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Chest Trauma Scoring Systems as Predictors of Morbidity and Mortality in Iraq

Study acronym: CTS
StatusNot Yet Recruiting
PhaseNot specified
Started
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Record status
This record was last updated March 19, 2025 (before its estimated June 10, 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Notable Start date: Feb 20, 2025 to Apr 20, 2025v4
  2. Notable Start date: Dec 20, 2024 to Feb 20, 2025
    • Primary completion date: Mar 10, 2025 to Jun 10, 2025
    • Study completion date: Mar 30, 2025 to Jun 30, 2025
    • Site contact updated
    v3
  3. Minor Secondary endpoint revisedv2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
This prospective observational study aims to evaluate the effectiveness of chest trauma scoring systems in predicting morbidity and mortality in patients with blunt chest trauma in Iraq. The primary questions it seeks to address are: How accurately do chest trauma scoring systems predict mortality and critical outcomes such as ICU admission or the need for advanced interventions? How well do these scoring systems stratify patients based on injury severity in a resource-limited setting? Are there any demographic or clinical factors that impact the predictive performance of these scoring systems? Participants will: Be assessed using chest trauma scoring systems upon arrival at the emergency department to determine risk levels. Have demographic and clinical data, including age, gender, injury mechanism, comorbidities, and length of hospital stay, collected to explore potential associations with outcomes.
Trial Details
NCT Number NCT06737575
Lead Sponsor Al-Nahrain University
Conditions
(from sponsor)
Chest Injury Trauma Blunt
Related terms Wounds and Injuries
Enrollment 190 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov