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NCT06860867 · ClinicalTrials.gov registry record · NA
PerQdisc Traditional Feasibility Trial.
A NA study of Discogenic Low Back Pain, sponsored by Spinal Stabilization Technologies.
- Recruiting
- Registry status
- NA
- Development phase
- 5
- Enrollment target
- 8
- Study locations
NCT06860867: Recruiting NA study of Discogenic Low Back Pain, sponsored by Spinal Stabilization Technologies.
NCT06860867 is a NA study of Discogenic Low Back Pain that is actively recruiting participants, run by Spinal Stabilization Technologies. The registered enrollment target is 5 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). The trial reports 8 study locations across 5 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06860867, a NA study of Discogenic Low Back Pain, is actively recruiting participants, sponsored by Spinal Stabilization Technologies.
- RECRUITING
- Registry status
- NA
- Development phase
- 5 participants
- Enrollment target
- 8
- Study locations
Study 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.
Primary Outcome
Clinical composite success is defined as improvement in pain and absence of qualified safety events.
Conditions Studied
Interventions
- DEVICE PerQdisc
Study Locations (8)
Arizona
- Hope Research Institute - Glendale
- The CORE Institute - Phoenix
- HOPE Research Institute - Phoenix
- HonorHealth Research & Innovation Institute - Scottsdale
Idaho
- Axis Spine Center - Coeur d'Alene
Indiana
- Indiana Spine Group - Carmel
Louisiana
- Spine Institute of Louisiana - Shreveport
Oklahoma
- SonoSpine - Oklahoma City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5 participants |
| Start Date | 2025-01-10 |
| Est. Completion | 2030-03-31 |
| Phase | NA |
What NCT06860867 shows while recruiting
NCT06860867 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
The record links to 1 condition, with Discogenic Low Back Pain appearing as the primary indexed condition, and to 1 intervention - of which PerQdisc is the first listed.
NCT06860867 lists 8 locations in 5 states (Arizona, Idaho, Indiana).
Frequently Asked Questions
What is clinical trial NCT06860867 about?
NCT06860867 is a clinical study titled "PerQdisc Traditional Feasibility Trial.". 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...
What is the current status of trial NCT06860867?
This trial is currently recruiting. It is a NA study. The enrollment target is 5 participants. The study started on 2025-01-10. Estimated completion is 2030-03-31.
What conditions does trial NCT06860867 study?
This clinical trial studies the following conditions: Discogenic Low Back Pain.
What interventions are being tested in trial NCT06860867?
The interventions under investigation include: PerQdisc (DEVICE).
Who is sponsoring clinical trial NCT06860867?
This trial is sponsored by Spinal Stabilization Technologies, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06860867 being conducted?
This trial has 8 study locations across Arizona, Idaho, Indiana, Louisiana, Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Discogenic Low Back Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT06860867's enrollment target sits among peer trials
5 1989th of 2000 higher than 5 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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