Analyzing the outcomes of patients with multiple trauma to improve emergency care
Official title: Collecting the Results of Physical Examination, Blood Test, and Radiological Examination of Multiple Trauma Patients With Activated Trauma Team and Understanding the Correlation With Patient's Morality and Mobility
Run by St. Martin De Porress Hospital · NCT06216873 · Data updated 2026-11-12
This study looks at data from trauma patients in the emergency room to see how different test results can help doctors improve care and outcomes for these patients.
Quick facts
| Study type | Observational |
|---|---|
| Sex | All |
| Enrollment | 400 (estimated) |
| Sponsor | St. Martin De Porress Hospital Academic / other |
| Locations | 2 sites (Chiayi City and 1 other locations) |
| Status | Recruiting |
| Started | December 29, 2023 |
| Main results expected | December 31, 2026 |
| Study ends | December 31, 2026 |
| Registry record updated | October 27, 2026 |
| Trial ID | NCT06216873 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients who have sustained multiple traumatic injuries and are admitted to the emergency department.
✕Probably not a fit
Patients who have expired upon arrival at the emergency room will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study collects and reviews data from patients admitted to the emergency department for major trauma. It focuses on physiological examination values, blood test results, and radiological findings to identify correlations between these parameters and patient outcomes. By analyzing medical records, the study aims to develop an effective assessment model that enhances rapid diagnosis and treatment evaluation for trauma patients. The ultimate goal is to improve emergency response and hospital resource allocation for better patient care.
Why it matters
Potential benefit: If successful, this study could lead to improved diagnostic and treatment protocols for patients with multiple trauma, potentially reducing mortality rates.
How similar studies have gone: While similar studies have explored trauma assessment models, this specific approach is novel in its focus on correlating multiple physiological parameters with patient outcomes.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria:multiple trauma patients - Exclusion Criteria:expired patients at emergency room \-
Where it's running
-
St. Martin De Porres Hospital
Chiayi City, Taiwan Recruiting -
St. Martin De Porres Hospital
Chiayi City, Taiwan Recruiting
Study contacts
- Principal investigator: Chia Hsi Chen, MD — Department of Emergency, St. Martin De Porres Hospital
- Study coordinator: Chia Hsi Chen, MD
- Email: urologist3509@gmail.com
- Phone: 886-5-2756000
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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-
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This study is trying to find out if a specific type of cell death related to iron is causing organ failure in critically ill patients in the ICU, to help develop new treatments in the future.
-
Comparing trauma scoring systems to predict mortality in trauma patients
This study is testing which of four trauma scoring systems can best predict survival chances for patients with injuries when they arrive at the emergency department.
-
Self-management program for recovery after traumatic injury
This study is testing a self-management program to help people recovering from serious injuries feel more confident and improve their daily lives.
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Using a smartphone app to track pain and mood changes
This study is testing a smartphone app to track pain and mood changes in people with chronic pain and healthy individuals to see how these factors affect pain over time.
-
Using whole blood for trauma patients with severe bleeding
This study tests whether using whole blood for trauma patients with severe bleeding can help them survive better and have fewer organ problems compared to traditional blood treatments.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.