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NCT Number: NCT07437989

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).

The study involves recording personal, clinical, and instrumental information. The acquisition of the above-mentioned personal and clinical information will be carried out in conjunction with the usual follow-up visits scheduled as part of normal clinical practice. At the end of the study, a statistical analysis of the data will be carried out.

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Key information

Conditions

Neuropathy Nervous System Diseases Neurologic Manifestations Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

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

Peschiera del Garda, Verona, 37019, Italy

Location status: Recruiting

Location contact

Giampietro Zanette, MD

CONTACT

[email protected]

+39 0456444193

About this study

Patients will be asked to participate in the prospective observational study after being fully informed of its objectives and how they will be pursued. Patient compliance is made official by signing the informed consent form.

Patients will then undergo nerve conduction tests and electromyography, as appropriate, and ultrasound evaluation as per clinical practice.

Prior to the above diagnostic investigations, patients will perform a neurological examination to assess the distribution and severity of neuropat

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients (age ≧ 18 years old) able to give consent
  • Diagnosis of peripheral nerve disorder

Exclusion criteria

  • The patient is unable to consent for him/herself

Treatment and study plan

peripheral neuropathies

Other

the neurophysiological study aimed at studying the function of nerves and nerve ultrasound to evaluate its morphological appearance will be performed. Depending on the outcome of the tests carried out, further blood tests will be ordered to identify the causes of neuropathy and identify the most effective treatment where available.

Primary outcomes

  1. record of all diagnosed peripheral neuropathies

    Time frame: through study completion, an average of 1 year

    The primary objective of the study is to make a record of all diagnosed peripheral neuropathies that systematically includes and collects demographic and clinical data (including data on diagnostic methods of an electrophysiological, imaging and laboratory nature) most relevant for the diagnostic and prognostic definition of such diseases.

Secondary outcomes

  1. assess the additional role of ultrasound in the diagnosis of diseases of the peripheral nervous system

    Time frame: through study completion, an average of 1 year

  2. Identifying ultrasound parameters of disease severity and/or treatment response

    Time frame: through study completion, an average of 1 year

Sponsors and collaborators

Lead sponsor

Casa di Cura Dott. Pederzoli

Other

Registry information

Official study title

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

Acronym: REG-NP

Important dates

Study start
2025
Primary completion
2035
Study completion
2035
First posted
Feb 27, 2026
Registry last updated
Feb 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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