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Study of the Long-Term Outcomes of Posterior Spinal Fixation With the Karma Device

Lumbar Disc Disease Clinical Trial

Official title:
CORTI-FIX: Clinical and Radiographic Outcomes Following Lumbar Interbody Placement With Posterior Minimally Invasive Intra-Laminar PEEK Ratcheting Fixation Device

Clinical Trial Summary

The primary objective of this clinical study is to measure fusion rate in patients at 12 months following lumbar fusion in combination with posterior fixation using the Karma® device.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04984213
Study type Observational
Source Spinal Elements
Contact
Status Not yet recruiting
Phase
Start date August 15, 2021
Completion date December 31, 2024
View Details
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