- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07812038
Predictive Value of Chest Trauma Score , Revised Trauma Score , and Glasgow Coma Scale in Patients Presenting With Chest Trauma at Assiut University Emergency Unit.
September 4, 2026 updated by: Tarek Ragaey Ali Sayed, Assiut University
Thoracic trauma is a critical clinical entity and a major global public health burden, representing the second most frequently occurring unintentional traumatic injury and the third most common cause of death-following head and abdominal injuries-in patients with polytrauma.
It places a substantial demand on emergency departments and directly accounts for 20% to 25% of all trauma-related fatalities worldwide(1).
The severity of these injuries is underscored by persistently high mortality rates, which can reach up to 60% in cases of severe blunt chest trauma depending on the healthcare setting.
Recent epidemiological data indicates that among potentially preventable trauma deaths, thoracic injuries represent up to 41%, with blunt mechanisms such as motor vehicle collisions acting as the primary driver (accounting for 80% to 92% of cases)(2).
Given this significant risk profile, rapid and accurate clinical triage is vital.
Current evidence consistently demonstrates that early recognition, protocolized multidisciplinary management, and the timely provision of definitive interventions at dedicated trauma centers are essential to decreasing morbidity and significantly reducing preventable trauma mortality(3).Effective initial assessment in the ED relies heavily on validated trauma scoring systems.
GCS is the most universally utilized tool for evaluating a patient's level of consciousness, calculating a score between 3 and 15 based on three physiological parameters: eye opening, verbal response, and motor response.
RTS is a broader physiological scoring system combining the GCS, systolic blood pressure, and respiratory rate.
CTS is a specific, targeted assessment tool designed to quantify the severity of thoracic injuries.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
100
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Probability Sample
Study Population
Patients with documented clinical or radiological evidence of chest injury (e.g., rib fractures, pulmonary contusion, pneumothorax, or hemothorax confirmed via X-ray, chest CT, or FAST).
Description
Inclusion Criteria:
- Age threshold: Patients aged 18 years and older (pediatric physiology requires entirely different trauma scoring systems).
- Mechanism of injury: Patients presenting with acute blunt or penetrating thoracic trauma or both.
- Diagnostic confirmation: Patients with documented clinical or radiological evidence of chest injury (e.g., rib fractures, pulmonary contusion, pneumothorax, or hemothorax confirmed via X-ray, chest CT, or FAST).
- Time of presentation: Patients presenting directly to the emergency department within 24 hours of the trauma incident.
Exclusion Criteria:
- Inter-facility transfers: Exclude patients transferred from other hospitals. If they were already intubated, given sedatives, or resuscitated elsewhere, their admission scores will be artificially altered and will not reflect their true initial presentation.
- Dead on Arrival (DOA): Patients who arrive in cardiac arrest or expire before the initial primary survey and scoring can be completed.
- Isolated severe head trauma or massive burns: Patients whose clinical picture and need for intubation are overwhelmingly driven by severe traumatic brain injury (e.g., GCS < 8 from head injury alone without significant chest trauma) or massive burns, rather than the thoracic injury.
- Severe chronic cardiopulmonary disease: patients with known end-stage COPD, severe baseline heart failure, or those on home oxygen. Their baseline hypoxia or need for ventilation can confound the trauma scores' predictive value.
- Incomplete data: Patients whose medical records are missing the crucial variables needed to calculate the GCS, RTS, or CTS upon arrival.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
study group
Patients with documented clinical or radiological evidence of chest injury (e.g., rib fractures, pulmonary contusion, pneumothorax, or hemothorax confirmed via X-ray, chest CT, or FAST
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
diagnositic acuracy of the Glasgow Coma Scale (GCS), in cases of thoracic trauma.
Time Frame: baseline
|
baseline
|
|
diagnostic acuracy of the Revised Trauma Score (RTS) in cases of thoracic trauma.
Time Frame: baseline
|
baseline
|
|
diagnostic acuracy of the Chest Trauma Score (CTS) in cases of thoracic trauma.
Time Frame: baseline
|
baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
October 1, 2026
Primary Completion (Estimated)
October 1, 2027
Study Completion (Estimated)
December 1, 2027
Study Registration Dates
First Submitted
September 4, 2026
First Submitted That Met QC Criteria
September 4, 2026
First Posted (Actual)
September 10, 2026
Study Record Updates
Last Update Posted (Actual)
September 10, 2026
Last Update Submitted That Met QC Criteria
September 4, 2026
Last Verified
September 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CTS ,RTS& GCS
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.