Spine device study ends early with only 4 patients

NCT ID NCT05489822

Terminated Knowledge-focused Sponsor: Silony Medical GmbH Source: ClinicalTrials.gov ↗

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

Summary

This study looked at the VERTICALE Cervical System, a device used to stabilize the spine during surgery. Researchers planned to track neck disability in patients with conditions like degenerative disc disease or trauma. Only 4 patients were enrolled before the study was terminated, so the findings are very limited.

What this could mean

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

Active substance: VERTICALE Cervical System (a medical device for spine stabilization)
What this could lead to: If successful, this study could confirm that the VERTICALE device improves neck function and pain after surgery, supporting its continued use.
What could go wrong: This was a very small study (only 4 patients) and was terminated early, so results may not be reliable or apply to others.

This is an AI summary of the original study and may miss details. Read our disclaimer.

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Conditions

The condition(s) this trial relates to.

Congenital Abnormalities injury intervertebral disk degenerative disorder lumbar disk degenerative disorder

As listed by the trial registrant

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

DEFORMITY DEGENERATIVE DISC DISEASE (DDD) INSTABILITIES TRAUMA

Contacts and locations

Locations

University of Illinois Hospital and Health Sciences System - UI Health

Chicago, Illinois, 60612, United States

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