Medicolegal Aspects of Traumatic Hand Injuries (hand-injuries)

December 1, 2025 updated by: Aya Mohamed Abdellah Ahmed, Sohag University

Medicolegal Aspects of Traumatic Hand Injuries in the Period From October 2025 to April 2026 in Sohag University Hospitals

The goal of this observational study is to assess and describe the epidemiology of traumatic hand injuries in Sohag University Hospital in different age group ,male, female with traumatic hand injury The main questions it aims to answer are:

what is the mechanism of injury ? what is the outcome of the injury ?

Study Overview

Status

Active, not recruiting

Detailed Description

The goal of this observational study is to assess and describe the epidemiology of traumatic hand injuries in Sohag University Hospital. study and analyze the medicolegal aspects of different traumatic hand injuries cases (patterns of injuries, mechanisms, causes, site of trauma and outcomes) in different age group ,male, female with traumatic hand injury The main questions it aims to answer are:

what is the mechanism of injury ? what is the Manner of Injury ? what is the outcome of the injury ? hs the injury affect the function of the hand ?

Study Type

Observational

Enrollment (Estimated)

100

Contacts and Locations

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

Study Locations

      • Sohag, Egypt
        • Sohag University hospitals

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

Probability Sample

Study Population

The study is specified in sohag university hospitals on patients with traumatic hand injuries

Description

Inclusion Criteria:

  • Diagnosed cases with traumatic hand and wrist injuries
  • Patient is willing to attend follow up appointments

Exclusion Criteria:

  • Patients with deficient data i.e. escaped, discharged on demand before period of follow up,…etc
  • Patient presented by life threating injuries in addition to hand injuries.
  • Patient with previous pathology in hand.

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
Diagnosed cases with traumatic hand and wrist injuries
Diagnosed cases with traumatic hand and wrist injuries of any age ,sex, educational level

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
assess the incidance of traumatic hand injuries in Sohag University Hospital in a period from October 2025 to April 2026
Time Frame: 6 months
6 months

Collaborators and Investigators

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

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)

October 1, 2025

Primary Completion (Estimated)

April 1, 2026

Study Completion (Estimated)

May 1, 2026

Study Registration Dates

First Submitted

September 19, 2025

First Submitted That Met QC Criteria

November 21, 2025

First Posted (Estimated)

December 3, 2025

Study Record Updates

Last Update Posted (Actual)

December 8, 2025

Last Update Submitted That Met QC Criteria

December 1, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • Soh-Med-25-9---21MS

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

Clinical Trials on Medicolegal Aspects

Subscribe