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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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
record of all diagnosed peripheral neuropathies
Timeframe: through study completion, an average of 1 year