Study of MRgFUS Exablate Treatment Following the Neuropathic Pain

Status Recruiting

Clinical Trial Summary

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 objectives of this study are to capture the change in pain intensity, physical/emotional function, and pain impact for patients diagnosed with neuropathic pain who undergo an Exablate treatment and to capture safety data of the procedure. The safety assessment measure is the incidence and frequency of device and procedure related Adverse Events (AEs) in subjects who undergo an Exablate treatment. Performance will be measure by assessing the change from baseline to 3 months post Exablate treatment for pain intensity defined as a decrease of at least 30% of pain on the Numeric Rating Scale (NRS). Assessing the change from baseline to 6-12 months post Exablate treatment for pain intensity assessed by using the Numeric Rating Scale (NRS) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04649554
Study type	Interventional
Source	InSightec
Contact	Khaja Rehman, PhD
Phone	+1 469 607 0497
Email	KhajaR@insightec.com
Status	Recruiting
Phase	N/A
Start date	October 8, 2020
Completion date	December 31, 2022

View Details

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