PerQdisc Traditional Feasibility Trial.
NCT06860867
This study is recruiting at 5 US sites in 4 states, according to its ClinicalTrials.gov record last updated .
Summary
This is a traditional feasibility study (TFS) study to evaluate the safety and effectiveness of the PerQdisc. The study is prospective, multicenter, and open label. After a screening period, qualified participants will be enrolled and treated with the PerQdisc. Patients will not be blinded to their treatment. Participants will then complete the safety follow-up period.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Discogenic Low Back Pain
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Not applicable
- Ages
- 22 to 70 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Sponsor
- Spinal Stabilization Technologies
- Last updated on ClinicalTrials.gov
- May 8, 2026
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Arizona · 2
- The CORE Institute · Phoenix, AZ
- HonorHealth Research & Innovation Institute · Scottsdale, AZ
Idaho · 1
- Axis Spine Center · Coeur d'Alene, ID
Indiana · 1
- Indiana Spine Group · Carmel, IN
Louisiana · 1
- Spine Institute of Louisiana · Shreveport, LA
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.