A Clinical Registry to Track the Real World Use of the Saber-C® Cervical Fusion Device
At a glance
Conditions
NCT06240221
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
Strenge Spine
Paducah, Kentuckyno site contact published
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
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Inclusion
Exclusion
What this trial measures
- Cervical spinal fusion status assessed via X-rays and CT scans1 year
Cervical spinal fusion status will be assessed via X-rays and CT scans at 1 year post-surgery
- Clinical outcome via neck visual analog scale (VAS)1 year
Standard of care patient reported neck visual analog scale (VAS) will be used to evaluate patient pain. On a scale of 0 to 10 with a score of 0 being no pain and a score of 10 being worst pain. A low score means a better clinical outcome. A high score means a worse clinical outcome.
- Clinical outcome via neck disability index (NDI)1 year
Standard of care patient reported neck disability index (NDI) will be used to evaluate patient pain and quality of life. On a vertical scale of 0 to 5 with a score of 0 meaning neck pain (if any) does not interfere with life activities and 5 meaning neck pain strongly interferes with life activities. A low score means a better clinical outcome. A high score means a worse clinical outcome.