Clinical Trials Directory

Trials / Unknown

UnknownNCT01933607

Post-market Study of the TOPS™ System

A Study to Evaluate the Safety and Effectiveness of the TOPS System

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
10 (estimated)
Sponsor
Premia Spine · Industry
Sex
All
Age
40 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The study is being conducted to evaluate look the TOPS System when used in patients with degenerative spondylolisthesis and lumbar spinal stenosis who would normally be candidates for spinal fusion.

Detailed description

This study is being conducted to evaluate the TOPS™ SP System from ("TOPS™ System" or "TOPS"). TOPS is an alternative to spinal fusion and is designed to stabilize but not fuse the affected vertebral level to alleviate pain stemming from degenerative spondylolisthesis (abnormal/excessive movement of the vertebrae causing pain in the lower back and legs) and spinal stenosis (narrowing of the spinal canal resulting in compression of nerves producing symptoms of pain, numbness and tingling in the legs).

Conditions

Interventions

TypeNameDescription
DEVICETOPS SystemNon-randomized study involving implantation of a TOPS via lumbar surgery to decompress and provide stability to the index level.

Timeline

Start date
2014-05-01
Primary completion
2016-12-01
Completion
2016-12-01
First posted
2013-09-02
Last updated
2016-04-18

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT01933607. Inclusion in this directory is not an endorsement.