Actively Recruiting
Comparative Analysis of MGAP and GAP Trauma Scores in Predicting Outcomes for Multiple Trauma Patients
Led by Al-Nahrain University · Updated on 2026-03-04
522
Participants Needed
1
Research Sites
112 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this prospective cohort study is to compare the predictive accuracy of the MGAP and GAP trauma scores in determining the prognosis of multiple trauma patients admitted to the emergency department at Al-Kadhimiya Teaching Hospital, Iraq. The main questions it aims to answer are: Does the MGAP score provide a more accurate prediction of outcomes compared to the GAP score? Are there specific subgroups of trauma patients where one score demonstrates superior predictive utility over the other? Participants will: Be assessed using both the MGAP and GAP scores upon admission to the emergency department. Have their clinical outcomes, including mortality, length of stay, and need for surgery, tracked throughout their hospital stay.
CONDITIONS
Official Title
Comparative Analysis of MGAP and GAP Trauma Scores in Predicting Outcomes for Multiple Trauma Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 16 years or older.
- Patients with multiple trauma involving two or more body regions or organ systems.
- Patients presenting to the emergency department within 6 hours of injury.
- Patients or their legal representatives provide informed consent to participate.
You will not qualify if you...
- Transfers from other facilities with prior interventions affecting score reliability.
- Pregnant women.
- Primary trauma caused by burn injuries.
- Incomplete medical records or failure to follow up.
- Patients deceased upon arrival at the emergency department.
- Patients who leave against medical advice.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
College of Medicine - Al-Nahrain University
Baghdad, Iraq
Actively Recruiting
Research Team
A
Abdulillah R. Khamees
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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