Follow-up of Post-spinal Implantable Neurostimulator PRECISION®

Cemka

Status: Completed

Conditions: Ischemic Peripheral Pain; Chronic Refractory Neuropathic Pain

Treatments: Device: Neurostimulator Precision

Study type: Observational

Funder types: Other; Industry

Identifiers

NCT02208999

2011045

913018 (Other Identifier)

Details and patient eligibility

About

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

Full 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

Enrollment: 106 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patient receiving spinal implantation of a neurostimulator PRECISION ® ( primary implantation or reimplantation)

Exclusion criteria

• Refusal of patient
• Patient whose long-term monitoring will not be possible

Trial design

106 participants in 1 patient group

Neurostimulator Precision

Description:

Patients implanted or reimplanted with the neurostimulator Precision

Treatment:

Device: Neurostimulator Precision