Analysis of Pediatric Trauma Registry Data:Patterns,Outcomes,and Predictors of Injury Severity.

January 21, 2026 updated by: Maria Wageh Youssef Fahem, Sohag University

Analysis of Pediatric Trauma Registry Data:Patterns,Outcomes, and Predictors of Injury Severity.

Type of the study: A prospective analytical observational study using pediatric trauma registry data.

Study period: The study will last for six months. Study setting: Sohag and Alexandria University Hospitals, Department of Emergency Medicine and pediatric surgery department .

Study Overview

Status

Not yet recruiting

Conditions

Detailed Description

Study subject:

Inclusion criteria:

  • Pediatric patients aged less than 18 years.
  • Presenting with any form of traumatic injury.

Exclusion Criteria:

  • Patients dead on arrival without available prehospital information.
  • Non-traumatic medical emergencies recorded in error.
  • pediatric patients presenting with burn.

Study Type

Observational

Enrollment (Estimated)

40

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 Locations

  • Egypt
      • Sohag, Egypt
        • Sohag University

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

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

Sohag and Alexandria University Hospitals, Department of Emergency Medicine and pediatric surgery department .

Description

Inclusion Criteria:

  • Pediatric patients aged less than 18 years.
  • Presenting with any form of traumatic injury.

Exclusion Criteria:

  • Patients dead on arrival without available prehospital information.
  • Non-traumatic medical emergencies recorded in error.
  • pediatric patients presenting with burn.

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
ICU admission rate.
Time Frame: Six months
The number and percentage of patients admitted to the intensive care unit during the index hospitalization among all eligible pediatric injury patients.
Six months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
length of hospital stay
Time Frame: Six months
Differences in length of hospital stay among injury types.
Six months

Collaborators and Investigators

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

Sponsor

Sohag University

Collaborators

Alexandria University

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)

February 1, 2026

Primary Completion (Estimated)

August 1, 2026

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

January 1, 2026

First Submitted That Met QC Criteria

January 21, 2026

First Posted (Actual)

January 28, 2026

Study Record Updates

Last Update Posted (Actual)

January 28, 2026

Last Update Submitted That Met QC Criteria

January 21, 2026

Last Verified

January 1, 2026

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • Soh-Med--25-12-12MS

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

I don't decide till now

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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