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Study of Exablate Model 4000 Type 1.0/1.1 Following the Treatment of Neuropathic Pain

Neuropathic Pain Clinical Trial

Official title:
Post Market Study of Exablate Model 4000 Type 1.0/1.1 Following the Treatment of Neuropathic Pain

Clinical Trial Summary

The Exablate 4000 obtained CE Mark for the treatment of Neuropathic Pain in December 2012. The purpose of this post market study is to obtain real world data on the safety and performance of the Exablate treatment for neuropathic pain. The objective of this study is to capture the change in pain intensity, physical/emotional function, and pain impact for patients diagnosed with neuropathic pain who undergo an Exablate treatment.

Clinical Trial Description

The purpose of this post market study is to obtain real world data on the safety and performance of the Exablate treatment for neuropathic pain. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05802511
Study type Interventional
Source IRCCS Centro Neurolesi "Bonino-Pulejo"
Contact
Status Completed
Phase N/A
Start date February 1, 2020
Completion date February 28, 2021
View Details
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