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.
Who can participate
Age range
22 Years – 60 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patient is skeletally mature and between 22 and 60 years of age.
* Patient has degenerative disc disease (DDD) at a single level between L1 and S1 as confirmed by:History and clinical findings suggestive of symptomatic DDD, Darkened disc on MRI in T2 weighted images, and decreased disc height (decreased greater than 2 mm compared to adjacent cranial or caudal disc height) with minimum disc height of 6 mm.
* Patient has pre-operative back pain VAS score of greater than or equal to 4 (0-10 scale).
* Patient has pre-operative Oswestry Low Back Disability score of greater than or equal to 40 (0-100 scale).
* Patient has received conservative (non-surgical) treatment for back pain for a minimum of 6 months.
* Patient has signed the approved Informed Consent Form.
Exclusion Criteria:
* Patient has had prior lumbar spine surgery.
* Patient has motion of less than 3 degrees on pre-operative lateral flexion/extension radiographs.
* Patient has ankylosing spondylitis or other spondyloarthropathy.
* Patient has isthmic spondylolisthesis or degenerative spondylolisthesis greater than 2 mm.
* Patient has congenital stenosis or epidural lipomatosis.
* Patient has significant facet disease.
* Patient has any known active malignancy.
* Patient has previously undergone immunosuppressive therapy.
* Patient has active local or system infection.
* Patient has been diagnosed with hepatitis, rheumatoid arthritis, lupus erythematosus, or other autoimmune disease, including …
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Rate of revision surgery at the treated level
Timeframe: 90 days
2
Rate of expulsion
Timeframe: 90 Days
3
Rate of new herniation at the treated level as determined by MRI
Timeframe: 90 days
4
Rate of new radiculopathy
Timeframe: 90 days
5
MRI assessment of the endplate Modic changes.
Timeframe: 90 days
6
Rate of surgical procedure technical success
Timeframe: 90 days
7
Improvement in degree of disability as measured by the Oswestry Disability Index (ODI)
Timeframe: 90 days
8
Improvement in back pain as measured by 10-centimeter Visual Analog Scale (VAS)