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Clinical Trial Summary

The investigators hypothesize that the association of I-ONE® therapy with standard rehabilitation treatment can optimize the clinical and functional recovery of patients with pulsed electromagnetic fields (PEMFs) (I-ONE® therapy) of the foot or ankle.


Clinical Trial Description

Study design; spontaneous, prospective, randomized study with control group. Purpose of the study: evaluate the functional clinical improvement of the foot/ankle joint with algodystrophic pathology following a standard rehabilitation treatment and home biophysical treatment and local biophysical stimulation with I-ONE® therapy (IGEA SpA). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05922618
Study type Interventional
Source Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Contact
Status Recruiting
Phase N/A
Start date August 1, 2023
Completion date June 1, 2027

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