"Evaluation of the Epidemiology of Surgically Treated Acute Traumatic Peripheral Nerve Injuries of the Upper Extremity and Their Long-Term Effects on Sensory and Motor, Functional Status, and Quality of Life"

May 8, 2026 updated by: Halenur Yaman, Suleyman Demirel University
Assessment of the Outcomes of Hand Nerve Injuries

Study Overview

Status

Recruiting

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 Contact

Study Locations

      • Isparta, Turkey (Türkiye), 32200
        • Recruiting
        • Süleyman Demirel Üniversitesi Uygulama ve Araştırma Hastanesi
        • Contact:
        • Contact:
          • halenur yaman

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

The study population consists of adult patients presenting with acute traumatic peripheral nerve injuries of the upper extremity, including median, ulnar, radial, and combined nerve injuries, who are evaluated and managed at a tertiary care university hospital.

Description

Inclusion Criteria:

  • Age 18 years and older
  • Diagnosis of acute traumatic peripheral nerve injury of the upper extremity (median, ulnar, radial, or combined injuries)
  • Injury requiring surgical or conservative management
  • Ability to provide informed consent

Exclusion Criteria:

  • History of previous peripheral nerve injury or surgery in the affected upper extremity
  • Presence of central nervous system disorders affecting upper extremity function
  • Severe concomitant musculoskeletal injuries preventing functional assessment
  • Inability to complete clinical and functional evaluations

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
ulnar nerve
Standard clinical and functional assessment of acute traumatic peripheral nerve injuries, including motor, sensory, and functional outcome evaluations, without assignment to a specific therapeutic intervention.
median nerve
Standard clinical and functional assessment of acute traumatic peripheral nerve injuries, including motor, sensory, and functional outcome evaluations, without assignment to a specific therapeutic intervention.
ulnar and median
Standard clinical and functional assessment of acute traumatic peripheral nerve injuries, including motor, sensory, and functional outcome evaluations, without assignment to a specific therapeutic intervention.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Michigan Hand Outcomes Questionnaire (MHQ) Total Score - Injured Hand
Time Frame: 6 months after injury
Patient-reported hand outcomes assessed with the Michigan Hand Outcomes Questionnaire (MHQ) for the injured hand. Total score range: 0-100; higher scores indicate better hand-related outcomes.
6 months after injury

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Grip Strength of Injured Hand (Jamar Dynamometer)
Time Frame: 6 months after injury
Grip strength of the injured hand measured using a Jamar dynamometer (kg). Mean of 3 trials; higher values indicate greater strength.
6 months after injury
Semmes-Weinstein Monofilament Test Threshold - Injured Hand
Time Frame: 6 months after injury
Cutaneous pressure threshold assessed using Semmes-Weinstein monofilaments in the injured hand. Reported as monofilament level (or gram-force, if applicable); lower values indicate better sensation.
6 months after injury
Static Two-Point Discrimination - Injured Hand
Time Frame: 6 months after injury
Static two-point discrimination measured in millimeters (mm) in the injured hand; lower values indicate better discrimination.
6 months after injury

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)

July 15, 2025

Primary Completion (Actual)

May 1, 2026

Study Completion (Estimated)

May 10, 2026

Study Registration Dates

First Submitted

January 28, 2026

First Submitted That Met QC Criteria

February 4, 2026

First Posted (Actual)

February 11, 2026

Study Record Updates

Last Update Posted (Actual)

May 13, 2026

Last Update Submitted That Met QC Criteria

May 8, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 104/15

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.

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