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Post Market Observational Trial for the PerQdisc Nucleus Replacement Device — PMCF1  

Degenerative Disc Disease Clinical Trial

Official title:
PerQdisc PMCF1 Observational Trial to Evaluate the Clinical Performance and Safety of the PerQdisc Nucleus Replacement Device

Clinical Trial Summary

PerQdisc PMCF1 is a post-market clinical follow-up observational trial to follow subjects receiving a PerQdisc spinal implant for a duration of 5 years.

Clinical Trial Description

This study will be a prospective, open-label, multi-center post-market observational study including 72 patients that will collect additional safety and efficacy data for the Spinal Stabilization Technologies PerQdisc Nucleus Replacement System. Primary endpoints will be used to assess the safety and efficacy of the PerQdisc device. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05105490
Study type Observational
Source Spinal Stabilization Technologies
Contact JEFFREY GRIEBEL
Phone +13032468241
Email jlgriebel@sstspine.com
Status Not yet recruiting
Phase
Start date December 31, 2021
Completion date October 31, 2027
View Details
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