Trauma Centers/Statistics & Numerical DatatraumaNCT07903727
Medical,Nursing Record,PE, Blood Test and Radiological Examination ,Morality and Mobility of Multiple Trauma Patient
An observational study of Trauma Centers/Statistics & Numerical Data and Trauma Blunt, run by St. Martin De Porress Hospital.
Trial summary
This study aims to analyze statistical data on physiological examination values, blood test results, and radiological findings in patients admitted to the emergency department for severe trauma. Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Trauma Centers/Statistics & Numerical Data, Trauma Blunt, Trauma (Including Fractures)
- What is being tested?
- Collect results of trauma patients
- Type of treatment
- Surgery or procedure
- How many people
- 700 participants
- Where
- No sites listed yet
- Study dates
- 1 Dec 2026to 31 Dec 2028
- How long will I take part?
- 12 Months
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Study population: Patients with severe trauma admitted to the emergency department
Who may be able to join
- severe trauma
- admitted to emergency department
Who cannot join
- incomplete clinical data
- lack of information in their medical records
- non-traumatic patients.
Trial locations and contacts
No sites are listed yet. Contact the study team or a site near you to ask about taking part.
About this study
Official title: Collect Results of Medical and Nursing Record,Physical Examination, Blood Test and Radiological Examination of Multiple Trauma Patients and Activated Trauma Team to Find the Correlation With Patient's Morality and Mobility
This study aims to analyze statistical data on physiological examination values, blood test results, and radiological findings in patients admitted to the emergency department for severe trauma. Given the diverse symptoms and varying mortality rates associated with severe trauma, this research seeks to understand and develop a feasible emergency department assessment model for rapid diagnosis and treatment assessment before the onset of severe trauma patients.
Read the detailed description
- This is a single-center retrospective study of patients admitted to the emergency department, primarily reviewing the medical records, emergency room observations, and patient examination findings.
- Starting in August 2025, the investigators collected data from patients who visited the hospital's emergency department from September 2015, focusing on retrospective medical records, hospital observations, and patient examination findings, including statistical analysis of physiological examination values, blood test values, and radiological examination results.
- This data can assist and remind attending physicians in the prognostic diagnosis of similar patients.
- This study will explore specific methods and effectiveness in improving the response of attending physicians to patients admitted with severe trauma.
- The benefits and economics of this operational model to increase the likelihood of accurate diagnosis and timely assessment of patients with severe trauma arriving at the emergency department, while also improving the quality of hospital staff allocation.
- Conditions
- Trauma Centers/Statistics & Numerical Data, Trauma Blunt, Trauma (Including Fractures), Trauma Abdomen, Trauma Chest
- Being tested
- Collect results of trauma patients
- Keywords
- physical examination, blood test, radiological examination, trauma, morality and mobility
- Medical subject headings
- Wounds, Nonpenetrating, Wounds and Injuries, Abdominal Injuries, Thoracic Injuries
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Collect results of trauma patientsProcedure or surgery
Collect results of medical and nursing record, physical examination, blood test and radiological examination of multiple trauma patients
| Study group | Role | What they receive |
|---|---|---|
| trauma | trauma with fracture, chest, abdomen, blunt Receives: Procedure: Collect results of trauma patients |
What is being measured
The primary outcome is the main question the study is designed to answer.
Collect results of trauma patients and find the correlation of patient's morality and mobility
Collect results of medical and nursing record, physical examination, blood test and radiological examination of multiple trauma patients and activated trauma team to find the correlation with patient's morality and mobility
Measured: From enrollment to the end of treatment at 12 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted29 Oct 2026
- Study start1 Dec 2026 (estimated)
- Primary completion31 Dec 2028 (estimated)
- Study completion31 Dec 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Trauma Centers/Statistics & Numerical DataStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Cross-sectional
- Enrolment
- 700 participants (estimated)
- Target duration
- 12 Months
Sponsor and investigators
- Lead sponsor
- St. Martin De Porress Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Chia-hsi Chen, St. Martin De Porress Hospital
- Investigators
- Chung-Jing Wang, professor, Study director, Institutional Review Board St. Martin De Porres Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07903727
- Sponsor's protocol ID
- 25B-024
- Acronym
- trauma
- Status last verified
- Nov 2026
- First submitted
- 22 Oct 2026
- Last updated
- 4 Nov 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: This is the private medical data
Study at a glance
From the registry record, last updated by the sponsor on 4 Nov 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Collect Results of Medical and Nursing Record,Physical Examination, Blood Test and Radiological Examination of Multiple Trauma Patients and Activated Trauma Team to Find the Correlation With Patient's Morality and Mobility
- ClinicalTrials.gov ID
- NCT07903727
- Acronym / sponsor ID
- trauma / 25B-024
- Conditions
- Trauma Centers/Statistics & Numerical Data, Trauma Blunt, Trauma (Including Fractures), Trauma Abdomen, Trauma Chest
- Keywords
- physical examination, blood test, radiological examination, trauma, morality and mobility
- Study type
- Observational
- Recruitment status
- Not yet recruiting
- Enrolment
- 700 participants (estimated)
- Lead sponsor
- St. Martin De Porress HospitalUniversity, hospital or other
- Study start
- 1 Dec 2026 (estimated)
- Primary completion
- 31 Dec 2028 (estimated)
- Study completion
- 31 Dec 2028 (estimated)
- First posted
- 29 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study aims to analyze statistical data on physiological examination values, blood test results, and radiological findings in patients admitted to the emergency department for severe trauma. Given the diverse symptoms and varying mortality rates associated with severe trauma, this research seeks to understand and develop a feasible emergency department assessment model for rapid diagnosis and treatment assessment before the onset of severe trauma patients.
Detailed description
- This is a single-center retrospective study of patients admitted to the emergency department, primarily reviewing the medical records, emergency room observations, and patient examination findings.
- Starting in August 2025, the investigators collected data from patients who visited the hospital's emergency department from September 2015, focusing on retrospective medical records, hospital observations, and patient examination findings, including statistical analysis of physiological examination values, blood test values, and radiological examination results.
- This data can assist and remind attending physicians in the prognostic diagnosis of similar patients.
- This study will explore specific methods and effectiveness in improving the response of attending physicians to patients admitted with severe trauma.
- The benefits and economics of this operational model to increase the likelihood of accurate diagnosis and timely assessment of patients with severe trauma arriving at the emergency department, while also improving the quality of hospital staff allocation.
Study design
- Observational model
- Case-control
- Time perspective
- Cross-sectional
- Target follow-up
- 12 Months
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| trauma | – | Procedure: Collect results of trauma patientstrauma with fracture, chest, abdomen, blunt |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Patients with severe trauma admitted to the emergency department
Key inclusion criteria (2 listed)
- severe trauma
- admitted to emergency department
Key exclusion criteria (3 listed)
- incomplete clinical data
- lack of information in their medical records
- non-traumatic patients.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Collect results of trauma patientsCollect results of medical and nursing record, physical examination, blood test and radiological examination of multiple trauma patients | Procedure or surgery | trauma |
Primary outcome
Collect results of trauma patients and find the correlation of patient's morality and mobility
Time frame: From enrollment to the end of treatment at 12 weeks
Collect results of medical and nursing record, physical examination, blood test and radiological examination of multiple trauma patients and activated trauma team to find the correlation with patient's morality and mobility
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Nov 2026.
- Individual participant dataSharing planned: No. This is the private medical data
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Chung-Jing Wang, professor study director
Institutional Review Board St. Martin De Porres Hospital
Questions about this trial
What is this clinical trial studying?
An observational study of Trauma Centers/Statistics & Numerical Data and Trauma Blunt, run by St. Martin De Porress Hospital.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 4 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Chia-Hsi Chen, physician (886-5-2756000 ext. 3708, stmirb3707@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Collect results of trauma patients and find the correlation of patient's morality and mobility (time frame: From enrollment to the end of treatment at 12 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Nov 2026.