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Clinical Trial Summary

Number of centres planned : 1 (CHU Nantes) Design : Randomized, Prospective Planning of the study : - Total duration: 34 months - Recruitment period: 24 months. - Follow-up time per patients : 7-10 months Expected number of cases : 12 Treatment, procedure, combination of procedures under consideration : During the study, patients will be implanted with the WAVEWRITER ALPHA™ system with the objective of decreasing patient pain with a spinal cord stimulation mode. There will be a random draw on the order of the stimulation program: - the tonic stimulation "LF": In tonic mode, the electrical stimulation of the sensory fibers of the posterior cords of the spinal cord induces local paresthesias - burst stimulation (or "burst") - high frequency" stimulation (1000 Hz) "High frequency: HF". - combined tonic + burst stimulation - combined tonic + high frequency stimulation


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05398003
Study type Interventional
Source Nantes University Hospital
Contact Sylvie RAOUL
Phone 02 40 16 50 80
Email sylvie.raoul@chu-nantes.fr
Status Recruiting
Phase N/A
Start date November 23, 2022
Completion date September 25, 2025

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