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Clinical Trial Summary

This is a prospective, multi-center, correlation study in which the investigators aim to explore the relationship between subjective pain questionnaires and the AdaptiveStim accelerometer output.


Clinical Trial Description

The aim of this research is to gather the necessary information relating to the patient his subjective self-report and the more objective information from the implanted IPG (RestoreSensor). Such subjective information can be gathered from the AdaptivStim output.

The main focus of this study is to explore the relationship between the subjective reporting of functional disability with the ODI, sleep quality with the Actiwatch and PSQI, pain intensity with the NRS-diary and the objective measurement of functional positions with the AdaptiveStim in patients receiving high density spinal cord stimulation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02974101
Study type Interventional
Source Universitair Ziekenhuis Brussel
Contact
Status Completed
Phase N/A
Start date November 2016
Completion date June 2017

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