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

November 1, 2026 updated by: Chia-hsi Chen, St. Martin De Porress Hospital

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.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

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.

Study Type

Observational

Enrollment (Estimated)

700

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Patients with severe trauma admitted to the emergency department

Description

Inclusion Criteria:

  • severe trauma
  • admitted to emergency department

Exclusion Criteria:

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

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

  • Observational Models: CASE_CONTROL
  • Time Perspectives: CROSS_SECTIONAL

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
trauma

trauma with fracture, chest, abdomen, blunt
Procedure: Collect results of trauma patients

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
From enrollment to the end of treatment at 12 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

St. Martin De Porress Hospital

Investigators

  • Study Director: Chung-Jing Wang, professor, Institutional Review Board St. Martin De Porres Hospital

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)

December 1, 2026

Primary Completion (Estimated)

December 31, 2028

Study Completion (Estimated)

December 31, 2028

Study Registration Dates

First Submitted

October 22, 2026

First Submitted That Met QC Criteria

October 22, 2026

First Posted (Actual)

October 29, 2026

Study Record Updates

Last Update Posted (Actual)

November 4, 2026

Last Update Submitted That Met QC Criteria

November 1, 2026

Last Verified

November 1, 2026

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 25B-024

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

This is the private medical data

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.

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