Actively Recruiting

Age: 16Years +
All Genders
NCT07186777

Comparison of EMTRAS, REMS, and GAP Scores in Trauma

Led by Al-Nahrain University · Updated on 2026-03-04

188

Participants Needed

1

Research Sites

65 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this prospective multicenter cohort study is to evaluate and compare the predictive utility of the EMTRAS, REMS, and GAP scores in determining key outcomes among trauma patients admitted to participating hospitals in Iraq. The primary outcomes of interest include mortality, the need for endotracheal intubation, and length of hospitalization. The main questions it aims to answer are: How accurately do EMTRAS, REMS, and GAP scores predict mortality in trauma patients? How effective are these scores in predicting the need for endotracheal intubation? How well do these scores correlate with hospitalization duration in trauma patients? Participants will: Be assessed using EMTRAS, REMS, and GAP scores upon admission to the emergency department. Have their clinical outcomes, including survival, intubation requirements, and length of hospital stay, monitored throughout their hospitalization.

CONDITIONS

Official Title

Comparison of EMTRAS, REMS, and GAP Scores in Trauma

Who Can Participate

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients presenting to the emergency department with trauma
  • Patients or their legal guardians must provide informed consent to participate in the study
  • Admission within 12 hours of injury
Not Eligible

You will not qualify if you...

  • Patients with incomplete clinical data or discharged before scoring can be performed
  • Pregnant patients
  • Patients who died before arrival or were declared dead on arrival
  • Patients who refuse participation or cannot provide informed consent

AI-Screening

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Trial Site Locations

Total: 1 location

1

College of Medicine - Al-Nahrain University

Baghdad, Iraq, 10001

Actively Recruiting

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Research Team

A

Abdulillah R. Khamees, MBBCH

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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