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A Study of Child Injury Based on Data Mining

ConditionsInjuriesChild
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age0-18
SponsorChildren's Hospital of Fudan University

About this trial

A comprehensive pediatric injury burden assessment is an essential foundation for formulating injury prevention strategies and improving emergency care for injured children. Although the hospital-based passive surveillance of national injury surveillance system of medical and health institutions has been well-established in China, the monitoring points of hospitals were not stratified according to children's hospital. Aim of the project is to collect epidemiological and clinical data to describe causes, clinical features and outcomes of pediatric injuries at a Children's Hospital in Shanghai, China. The project intends to establish a method for collecting and analyzing high quality data of child injury using data mining based on the hospital information system.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

pediatric patients between the ages of 0-18 years newly diagnosed with injuries

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • not applicable (Observational Study)

    Other intervention

    This is an observational study and does not include interventions.

Treatment groups

10,762 Participants
are divided into 1 treatment group
Group A: Child injuries1 intervention

Trial outcomes

Primary outcomes

1

Distribution of injury categories

According to the electronic medical record system, the distribution of injury categories is defined as the proportion of various injury causes (fall，motor vehicle crash，sports, struck, foreign body) in the cohort subjects.

Time frame
At baseline

Secondary outcomes

1

28 days mortality

Mortality within 28 days from Emergency Department（ED）admission based on electronic medical records system

Time frame
Within 28 days from ED admission
2

180 days mortality

Mortality based on electronic medical records system

Time frame
Within 180 days from ED admission
3

Short-term disability

Disability accessed by the Glasgow Outcome Scale (GOS) at 180 days from ED admission. The Glasgow Outcome Scale was dichotomized into favorable outcome (moderate disability or good recovery ; GOS score of 4 or 5) and unfavorable outcome (death, vegetative state or severe disability; GOS score 1-3).

Time frame
At 180 days from ED admission
4

Percentage of ICU admission

Percentage of ICU admission from ED admission to 72 hours based on electronic medical records system

Time frame
From ED admission to 72 hours

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Children's Hospital of Fudan University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: