Examination of Nociscan Impact on Discogenic Low Back Pain Surgical Outcomes
← catalyst calendarNCT06661850 · readout in 407 d
Sponsored by Aclarion (industry) · ACON — their whole pipeline →. With MCRA.
Phase
—
Status
Recruiting
Study type
Observational
Enrollment
300estimated
Sites
9
Country
United States
Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →
Source: ClinicalTrials.gov, retrieved 2026-08-19
Dates
each axis at the precision it was filed, with the registry's own basis| Date | Filed | Basis | What it is |
|---|---|---|---|
| Start | 2025-06-11 | actual | When the study began enrolling |
| Primary completion | 2027-09-30 | estimated | The date the last participant is measured for the primary outcome — the readout window |
| Study completion | 2027-12-31 | estimated | The whole study's end, after follow-up |
| First posted | 2024-10-28 | actual | When this record first appeared on the registry |
| Results posted | — | When the sponsor posted results to the registry | |
| Record updated | 2026-07-24 | actual | The sponsor's own last edit to this record — every projection above is as current as this date |
What it studies
Condition
- Discogenic Low Back Pain
Intervention
- Procedure: Fusion or TDR determined by investigator.
Primary outcome
what the primary-completion date above is the date OFChange in back pain on 100mm Visual Analog Scale (VAS) Pain Assessment
measured Baseline to 12 months
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