New spinal implant shows promise for chronic back pain

NCT ID NCT04416321

First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested a special spinal implant (the Keos Lumbar Interbody Fusion Device) in 25 adults with degenerative disc disease or related spine conditions. The goal was to see how well the device helped bones fuse and how it affected pain and quality of life. Participants had spinal fusion surgery using the device, and results were tracked over time.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

Keos Lumbar Interbody Fusion Device (a spinal implant made of PEEK-OPTIMA HA enhanced material)

What this could lead to

If successful, this device could provide a safe and effective option for spinal fusion surgery, potentially reducing back pain and improving quality of life.

What could go wrong

This is a small, single-center study with only 25 participants and no comparison group. Results may not apply to all patients, and the device may not perform better than existing options.

Disclaimer Read more

This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Conditions

The condition(s) this trial relates to.

intervertebral disk degenerative disorder lumbar disk degenerative disorder spondylolisthesis

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Neurosurgical Associates of Lancaster

    Lancaster, Pennsylvania, 17601, United States