Serum sRAGE, CC16, and Syndecan-1 as Predictors of ARDS and Mortality After Severe Chest Trauma
NCT07774338
Acute Respiratory Distress Syndrome, Chest Trauma
View Trial DetailsNCT Number: NCT07812038
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.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: baseline
Time frame: baseline
Time frame: baseline
Assiut University
Other
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