An observational study in Neuropathy, sponsored by Casa di Cura Dott. Pederzoli. Recruiting at 1 site in Italy. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-27.
Sponsored by Casa di Cura Dott. Pederzoli · Observational
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.
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
198 studies on the registry are indexed under Neurologic Manifestations; 67 are open to participants now.
This study's planned enrollment of 4,000 is above the median of 184 across 82 observational studies indexed under Neurologic Manifestations.
Browse Neurologic Manifestations studies →Casa di Cura Dott. Pederzoli is the lead sponsor of 15 studies on the registry; 13 are open to participants now.
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recording all diagnosed peripheral neuropathies of P. Pederzoli Hospital in order to systematically collect demographic and clinical data (including data on diagnostic methods of an electrophysiological, imaging and laboratory nature)
Exclusion Criteria:
1. The patient is unable to consent for him/herself
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.
record of all diagnosed peripheral neuropathies
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.
Time frame: through study completion, an average of 1 year
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
Plan to share: No
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Casa di Cura Dott. Pederzoli