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Single Center Study Comparing MOBIS II ST vs MOBIS PEEK — MOBIS_US  

Lumbar Disc Disease Clinical Trial

Official title:
Prospective, Randomized, Data Registry Study of MOBIS II Structural Titanium (ST) Interbody Cage Compared to MOBIS Peek Cage for the Treatment of Spondylolisthesis and Degenerative Disc Disease

Clinical Trial Summary

Prospective randomized clinical study comparing SIGNUS MOBIS PEEK vs SIGNUS MOBIS II ST in patients with Degenerative Disc Disease at one or two contiguous levels from L2-S1

Clinical Trial Description

The protocol includes skeletally mature patients both male and female, 18 to 89 years old, with degenerative disc disease (DDD) at one or two contiguous levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients may also have up to a Grade I spondylolisthesis or retrolisthesis at the involved level(s). Patient should have completed at least six (6) months of non-operative treatment. Patients may have had a previous non-fusion surgery at the involved spinal level(s) and will be followed clinically up to two years. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02852187
Study type Interventional
Source Signus Medizintechnik GmbH
Contact
Status Withdrawn
Phase N/A
Start date July 2016
Completion date November 2018
View Details
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