Stopped: Trial was terminated prematurely due to receipt of CE mark
This study will be a prospective, open-label, multi-center study that will collect safety data for the minimally invasive PerQdisc Nucleus Replacement Device deployed to reduce chronic low back pain.
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Rate of revision surgery at the treated level
Timeframe: 90 days
Rate of expulsion
Timeframe: 90 Days
Rate of new herniation at the treated level as determined by MRI
Timeframe: 90 days
Rate of new radiculopathy
Timeframe: 90 days
MRI assessment of the endplate Modic changes.
Timeframe: 90 days
Rate of surgical procedure technical success
Timeframe: 90 days
Improvement in degree of disability as measured by the Oswestry Disability Index (ODI)
Timeframe: 90 days
Improvement in back pain as measured by 10-centimeter Visual Analog Scale (VAS)
Timeframe: 90 days