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Clinical Trial Summary

This post-marketing monocentric double-blind sham controlled crossover study will assess the efficacy of Rebox electrotherapy in the treatment of pain. Totally 72 patients will be treated with both real and sham Rebox device in a crossover design with a 1:1 ratio over a 6-week period. The degree of pain intensity reduction after the real Rebox stimulation will be evaluated in comparison with the sham stimulation. Moreover, differences in multidimensional aspects of pain will be compared between the real and sham stimulation.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05968274
Study type Interventional
Source Rebox Therapy s.r.o.
Contact Matej Slovák, MD, PhD
Phone +420605909750
Email matej.slovak@rebox.cz
Status Recruiting
Phase Phase 4
Start date October 1, 2023
Completion date May 10, 2024

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