- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07402655
"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
Conditions
Intervention / Treatment
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
- Name: halenur yaman
- Phone Number: +905418758844
- Email: halenurayvaci@sdu.edu.tr
Study Locations
-
-
-
Isparta, Turkey (Türkiye), 32200
- Recruiting
- Süleyman Demirel Üniversitesi Uygulama ve Araştırma Hastanesi
-
Contact:
- halenur yaman
- Phone Number: +905418758844
- Email: hale_ayvaci@hotmail.com
-
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.
Sponsor
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
Additional Relevant MeSH Terms
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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