Collecting the Results of Multiple Trauma Patients and Find the Correlation of Morality and Mobility (trauma)

January 19, 2024 updated by: St. Martin De Porress Hospital

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

Collect data about physiological examination values, blood test values and radiological examination results of patients admitted to the hospital for major trauma. There are different causes of mortality in multiple trauma patients. In this study, review the multiple symptoms and parameters of major trauma patients. We hope to understand and develop one feasible assessment model for emergency departments for enable rapid diagnosis and treatment evaluation about major trauma patients occurrence.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

  1. This is a retrospective study of patients admitted to the emergency department at a single center, focusing on reviewing their medical records and patient examination performance.
  2. The parameters including hospital on-site records and patient examination result, physiological examination values, blood test values and radiological examination results.on the medical records of patients who visited emergency department are collected.
  3. This study will explore how to improve the response and effectiveness of investigating patients when they are admitted to the hospital for major trauma.
  4. Evaluate the effectiveness and efficiency of this operative model to increase the possibility of receiving medical examination, timely correct diagnosis on major trauma patients when they sent to the emergency department, and improve the hospital's manpower deployment plan.

Study Type

Observational

Enrollment (Estimated)

350

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

Study Locations

      • Chiayi City, Taiwan, 60069
        • Recruiting
        • St. Martin De Porres Hospital
        • Contact:
      • Chiayi City, Taiwan, 600046
        • Recruiting
        • St. Martin De Porres Hospital
        • Contact:

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

Sampling Method

Non-Probability Sample

Study Population

The multiple trauma patients are sent to emergency room for further evaluation and management.

Description

Inclusion Criteria:multiple trauma patients -

Exclusion Criteria:expired patients at emergency room

-

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
multiple trauma
multiple trauma patients sent to emergency room for further evaluation are included
Review the medical record to gather the physical parameters, blood examination result and radiologic examination results

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Survey of Mortality and Mobility on Multiple Trauma Patients
Time Frame: 20100101 till 20241231
Analyze and evaluate the effectiveness of this operative model to increase the possibility of correct diagnosis and timely medical examination major trauma patients and improve the hospital's manpower deployment plan.
20100101 till 20241231

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Chia Hsi Chen, MD, Department of Emergency, 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 (Actual)

December 29, 2023

Primary Completion (Estimated)

December 28, 2024

Study Completion (Estimated)

January 31, 2025

Study Registration Dates

First Submitted

January 11, 2024

First Submitted That Met QC Criteria

January 19, 2024

First Posted (Actual)

January 22, 2024

Study Record Updates

Last Update Posted (Actual)

January 22, 2024

Last Update Submitted That Met QC Criteria

January 19, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 23B-021

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The individual participant data include the personal medical data and should not be shared with other researchers.

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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