NCT02208999

Follow-up of Post-spinal Implantable Neurostimulator PRECISION®

Two-years Follow-up of Post-spinal Implantable Neurostimulator PRECISION®

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 106 (actual)
• Sponsor: Cemka-Eval · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

Assessing the long-term efficacy, complications, revision rates and final explantation of the device

Detailed description

Longitudinal study with a follow-up of 2 years in patients implanted with the Precision neurostimulator. This study will describe the characterisrics of the patients, of the implantation and will assess the long-term efficacy, complications, revision rates and final explantation of the device

Conditions

• Chronic Refractory Neuropathic Pain
• Ischemic Peripheral Pain

Interventions

Type	Name	Description
DEVICE	Neurostimulator Precision	All patients included must have been implanted with the neurostimulator Precision

Timeline

• Start date: 2013-12-01
• Primary completion: 2017-12-01
• Completion: 2017-12-01
• First posted: 2014-08-05
• Last updated: 2019-11-06
• Results posted: 2019-11-06

Locations

1 site across 1 country: France