Actively Recruiting
Thorax vs. Trauma Injury Severity Scores as Outcome Predictors in Chest Trauma
Led by Al-Nahrain University · Updated on 2026-03-04
150
Participants Needed
1
Research Sites
99 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this observational study is to compare the predictive utility of the Thorax Trauma Severity Score (TTSS) and the Trauma and Injury Severity Score (TRISS) in determining outcomes among patients presenting with chest trauma to the emergency room. The main questions it aims to answer are: Does the TTSS provide a more accurate prediction of patient outcomes (e.g., mortality, ICU admission) than the TRISS? Are there specific patient subgroups where one score is more effective than the other? Participants will: Have their chest trauma severity assessed using both TTSS and TRISS during their emergency room admission. Have their clinical outcomes (e.g., mortality, ICU admission, length of hospital stay) monitored throughout their hospital stay.
CONDITIONS
Official Title
Thorax vs. Trauma Injury Severity Scores as Outcome Predictors in Chest Trauma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with chest injuries that require clinical assessment using the Thorax Trauma Severity Score (TTSS) and the Trauma Injury Severity Score (TISS) within 6 hours of admission.
- Patients (or their legal guardians) must provide informed consent for participation in the study.
- Patients presenting with thoracic injuries, including rib fractures, pulmonary contusions, pneumothorax, hemothorax, and other chest-related injuries, including isolated chest trauma and multiple injuries.
You will not qualify if you...
- Patients younger than 16 years.
- Patients with chest injuries caused by conditions unrelated to trauma, such as spontaneous pneumothorax, infections, or other medical conditions like non-traumatic rib fractures or cancer.
- Patients with severe co-morbidities such as terminal illnesses, advanced cancer, or end-stage organ failure.
- Patients with pre-existing severe neurological conditions or other comorbidities that interfere with trauma assessment and management.
- Patients or their legal representatives who refuse consent for participation.
- Pregnant women due to potential risks associated with trauma and interventions during pregnancy.
AI-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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