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Recruiting 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"

Observational Nerve Damage Trauma Nervous System

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Peripheral Nerve Injury Assessment.
Who it may be relevant to
Registry conditions: Nerve Damage, Trauma Nervous System. Basic parameters: 18 years — 80 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Assessment of the Outcomes of Hand Nerve Injuries

Interventions

  • Other Peripheral Nerve Injury Assessment
    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.

Primary outcome measures

  • Michigan Hand Outcomes Questionnaire (MHQ) Total Score - Injured Hand [Time frame: 6 months after injury]
Secondary outcome measures (3)
  • Grip Strength of Injured Hand (Jamar Dynamometer) [Time frame: 6 months after injury]
  • Semmes-Weinstein Monofilament Test Threshold - Injured Hand [Time frame: 6 months after injury]
  • Static Two-Point Discrimination - Injured Hand [Time frame: 6 months after injury]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Turkey (Türkiye) · 1 center
  • Süleyman Demirel Üniversitesi Uygulama ve Araştırma Hastanesi — Isparta

Identifiers

NCT: NCT07402655 · 104/15

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗