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Recruiting 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).

Observational Neuropathy

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 neuropathies.
Who it may be relevant to
Registry conditions: Neuropathy. Basic parameters: from 18 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
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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.

Detailed description

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

Interventions

  • Other peripheral neuropathies
    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 outcome measures

  • record of all diagnosed peripheral neuropathies [Time frame: through study completion, an average of 1 year]
Secondary outcome measures (2)
  • 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]
  • Identifying ultrasound parameters of disease severity and/or treatment response [Time frame: through study completion, an average of 1 year]

Eligibility criteria

Inclusion criteria

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

Exclusion criteria

1\. The patient is unable to consent for him/herself

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
Case-only

Study locations

Italy · 1 center
  • Ospedale P. Pederzoli Casa di Cura Privata S.p.A. — Peschiera del Garda

Identifiers

NCT: NCT07437989 · 417CET

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗