Actively Recruiting

Age: 18Years +
All Genders
ID07437989

An Observational Prospective Study on Patients With Peripheral Neuropathies Explored With Combined Clinical, Neurophysiological, and Nerve Ultrasound Approach

Led by Casa di Cura Dott. Pederzoli · Updated on 2026-02-27

4000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This observational study focuses on patients with peripheral neuropathies to collect detailed demographic, clinical, and instrumental data. It aims to explore nerve function and morphology through neurological examinations, nerve conduction studies, electromyography, and ultrasound evaluations. The goal is to better understand peripheral nerve disorders and evaluate the added role of ultrasound in diagnosis and disease severity assessment. Participants will undergo neurological exams and neurophysiological tests including nerve conduction and electromyography, followed by ultrasound assessments as part of routine clinical practice. Depending on test results, additional blood tests may be performed to identify causes of neuropathy and guide treatment decisions. Data collection will happen alongside usual follow-up visits. During the study, researchers will record all diagnosed peripheral neuropathies and analyze ultrasound parameters related to disease severity and treatment response. Patient compliance is confirmed through informed consent. The study will last about one year on average, with data analyzed statistically at the end to better understand peripheral nerve disorders.

CONDITIONS

Brief Title

Collection of Demographic, Clinical, and Instrumental Data of Patients With Peripheral Neuropathy Including Neurological Examination Data, Peripheral Nerve Conduction Analysis, and Nerve Electromyography and Ultrasound).

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients (age �3e�3d 18 years) able to give consent
  • Diagnosis of peripheral nerve disorder
Not Eligible

You will not qualify if you...

  • Unable to give consent for themselves

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Up to 1 year

Participants undergo neurological examination, nerve conduction tests, electromyography, and ultrasound evaluation as part of clinical practice to assess peripheral neuropathies.

Visits as per clinical practice

Long-term Monitoring

Duration - Up to 1 year

Participants are observed over time to record diagnoses, assess ultrasound's role in diagnosis, and identify parameters of disease severity or treatment response.

Follow-up visits as determined by clinical need

Trial Site Locations

Total: 1 location

1

Ospedale P. Pederzoli Casa di Cura Privata S.p.A.

Peschiera del Garda, Verona, Italy, 37019

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How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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