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A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditional SCS Systems — SCS MRI PMCF  

Chronic Pain Clinical Trial

Official title:
A Post-Market Study Evaluating the Prodigy MRI and Proclaim Elite MR Conditional SCS Systems

Clinical Trial Summary

A post market study evaluating the safety of the Prodigy MRI and Proclaim Elite MR conditional Spinal Cord Stimulator (SCS) systems.

Clinical Trial Description

The study will be performed as an international, multicenter, prospective and single-arm design. The study will be conducted as a Post Market Clinical Follow Up (PMCF) study and the results will be submitted to the Notified Body: BSI Group (BSI). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02738840
Study type Interventional
Source Abbott Medical Devices
Contact
Status Completed
Phase N/A
Start date October 21, 2016
Completion date December 2, 2020
View Details
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