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Not yet recruitingNCT07903727traumaUpdated Nov 4, 2026

Medical,Nursing Record,PE, Blood Test and Radiological Examination ,Morality and Mobility of Multiple Trauma Patient

An observational study in Trauma Centers/Statistics & Numerical Data, Trauma Blunt and Trauma (Including Fractures), sponsored by St. Martin De Porress Hospital. Not yet recruiting. Per ClinicalTrials.gov, last updated 2026-11-04.

Sponsored by St. Martin De Porress Hospital · Observational

Updated Nov 4, 2026Eligibility revisedTitle changed+2 moreGo to Updates ↓
Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
700
Sex
All
01

Study 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. 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
  1. 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.
  2. 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.
  3. This data can assist and remind attending physicians in the prognostic diagnosis of similar patients.
  4. This study will explore specific methods and effectiveness in improving the response of attending physicians to patients admitted with severe trauma.
  5. 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.
02

Conditions studied

  • 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
03

In context

Wounds, Nonpenetrating

37 studies on the registry are indexed under Wounds, Nonpenetrating; 11 are open to participants now.

This study's planned enrollment of 700 is above the median of 150 across 21 observational studies indexed under Wounds, Nonpenetrating.

Browse Wounds, Nonpenetrating studies →

Lead sponsor

St. Martin De Porress Hospital is the lead sponsor of 11 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

The criteria were revised on the registry on Nov 4, 2026. See what changed

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients with severe trauma admitted to the emergency department

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • severe trauma
  • admitted to emergency department

Exclusion criteria

Exclusion Criteria:

  • incomplete clinical data
  • lack of information in their medical records
  • non-traumatic patients.
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
700 participants (estimated)
Target follow-up
12 Months
Patient registry
Yes

Groups and cohorts

  • trauma

    trauma with fracture, chest, abdomen, blunt

    Procedure: Collect results of trauma patients

Interventions

  • ProcedureCollect results of trauma patients

    Collect results of medical and nursing record, physical examination, blood test and radiological examination of multiple trauma patients

06

What researchers measure

Primary outcomes

  1. 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

    Time frame: From enrollment to the end of treatment at 12 weeks

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: No — This is the private medical data

No publications or documents are linked to this record.

09

Updates

3 registry updates since Sep 25, 2026
Eligibility
Criteria revised in 2 updates
What changed on Nov 2, 2026
  • EditedInclusion Criteria: A single-center retrospective study of patients with severe trauma admitted to the emergency department
  • EditedExclusion Criteria: Excluding patients with incomplete clinical data, lack of information in their medical records, and non-traumatic patients.
What changed on Nov 4, 2026
Inclusion criteria
  • Addedsevere trauma
  • EditedInclusion Criteria: severe trauma admitted to the emergency department
Exclusion criteria
  • Addedincomplete clinical data
  • EditedExclusion Criteria: incomplete clinical data lack of information in their medical records non-traumatic patients.
  • Addednon-traumatic patients.
across 2 updates, Nov 2, 2026 – Nov 4, 2026
Contact
Study contact changed: s•••@gmail.com · •••6000→s•••@gmail.com · •••6000. See the current contact
Nov 2, 2026
Title
Results of Medical and Nursing Record,Physical Examination, Blood Test and Radiological Examination of Multiple Trauma to Find the Correlation With Patient's Morality and Mobility→Medical,Nursing Record,PE, Blood Test and Radiological Examination ,Morality and Mobility of Multiple Trauma Patient
across 2 updates, Nov 2, 2026 – Nov 4, 2026
Registered
First appeared on the registry
Oct 29, 2026
Show all 3 updates
  1. Nov 4, 2026
    Eligibility 1 inclusion criterion edited, 1 added; 1 exclusion criterion edited, 2 added
    What changed in the criteria
    Inclusion criteria
    • Addedsevere trauma
    • EditedInclusion Criteria: severe trauma admitted to the emergency department
    Exclusion criteria
    • Addedincomplete clinical data
    • EditedExclusion Criteria: incomplete clinical data lack of information in their medical records non-traumatic patients.
    • Addednon-traumatic patients.
    Title Results of Medical and ,Nursing Record,PE, Blood Test and Radiological Examination ,Morality and Mobility of Multiple Trauma of Patient's
    + 1 other change: verification date
  2. Nov 2, 2026
    Eligibility 2 criteria edited
    What changed in the criteria
    • EditedInclusion Criteria: A single-center retrospective study of patients with severe trauma admitted to the emergency department
    • EditedExclusion Criteria: Excluding patients with incomplete clinical data, lack of information in their medical records, and non-traumatic patients.
    Contact Study contact changed: s•••@gmail.com · •••6000→s•••@gmail.com · •••6000. See the current contact
    Title Results of Medical and Nursing Record,Physical ExaminationPE, Blood Test and Radiological Examination ,Morality and Mobility of Multiple Trauma to Find the Correlation Withof Patient's Morality and Mobility
    + 1 other change: description
  3. Oct 29, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07903727
Lead sponsor
St. Martin De Porress Hospital
Responsible party
Chia-hsi Chen (Emergency Medicine physcian, St. Martin De Porress Hospital) — Principal investigator
First posted
Oct 29, 2026
Start date
Dec 1, 2026 (estimated)
Primary completion
Dec 31, 2028 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Nov 4, 2026

Study contacts

Chia-Hsi Chen, physician
Contact
stmirb3707@gmail.com
886-5-2756000 ext. 3708
Chung-Jing Wang, professor
Contact
stmirb3707@gmail.com
886-5-2756000 ext. 3708
Chung-Jing Wang, professor
study director · Institutional Review Board St. Martin De Porres Hospital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Nov 2026. You cannot join it, but the record below documents what was studied.

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